Oncolytic adenovirus

ABSTRACT

Viral vectors and methods of making such vectors are described that preferentially kill neoplastic but not normal cells, the preferred vector being an adenovirus that has the endogenous promoters in the E1A and/or E4 regions substituted with a tumor specific promoter which is preferably E2F responsive.

FIELD OF THE INVENTION

[0001] This application is a continuation-in-part of U.S. patentapplication Ser. No. 10/303,598 filed Nov. 25, 2002, which is acontinuation-in-part of U.S. patent application Ser. No. 09/714,409filed Nov. 14, 2000, which in turn claims priority from U.S. ProvisionalApplication No. 60/165,638, filed Nov. 15, 1999.

[0002] This invention relates to adenovirus vectors, and to methods formaking and using such vectors. More particularly, it relates to improvedadenovirus vectors containing mutations and substitutions in thepromoters of the E1A and/or the E4 regions which confer substantialtumor cell specific oncolytic activity.

BACKGROUND

[0003] From the early part of this century, viruses have been used totreat cancer. The approach has been two-fold; first, to isolate orgenerate oncolytic viruses that selectively replicates in and killneoplastic cells, while sparing normal cells. Investigators initiallyused wild type viruses, and this approach met with some, albeit, limitedsuccess. While oncolysis and slowing of tumor growth occurred withlittle or no damage to normal tissue, there was no significantalteration in the course of the disease. See, Smith et al., Cancer 9:1211-1218 (1956), Cassel, W. A. et al., Cancer 18: 863-868 (1965), Webb,H. E. et al., Lancet 1: 1206-1209 (1966). See, also, Kenney, S andPagano, J. J. Natl. Cancer Inst., vol. 86, no. 16, p.1185 (1994).

[0004] More recently, and because of the reoccurrence of diseaseassociated with the limited efficacy of the use of wild type viruses,investigators have resorted to using recombinant viruses that can bedelivered at high doses, and that are replication competent inneoplastic but not normal cells. Such viruses are effective oncolyticagents in their own right, and further, can be engineered to carry andexpress a transgene that enhances the anti neoplastic activity of thevirus. An example of this class of viruses is an adenovirus that ismutant in the E1B region of the viral genome. See, U.S. Pat. No.5,677,178, and Bischoff, J. R., D. H. Kim, A. Williams, C. Heise, S.Horn, M. Muna, L. Ng, J. A. Nye, A. Sampson-Johannes, A. Fattaey, and F.McCormick. 1996, Science. 274:373-6.

[0005] It is important to distinguish the use of replication competentviruses, with or without a transgene for treating cancer, from thesecond approach that investigators have used, which is a non-replicatingvirus that expresses a transgene. Here the virus is used merely as avehicle that delivers a transgene which, directly or indirectly, isresponsible for killing neoplastic cells. This approach has been, andcontinues to be the dominant approach of using viruses to treat cancer.It has, however, met with limited success, and it appears to be lessefficacious than replicating viruses. Nevertheless, foreign genes havebeen inserted into the E1 region (see McGrory, Virology 163: 614-17(1988)), the E3 region (see Hanke, Virology 177: 437-44 (1990) and Bett,J. Virol. 67: 5911-21 (1993)) or into the E3 region of an E1 deletedvector.

[0006] As mentioned above, to avoid damage to normal tissues resultingfrom the use of high dose viral therapy it is preferred that the virushave a mutation that facilitates its replication, and hence oncolyticactivity in tumor cells, but renders it essentially harmless to normalcells. This approach takes advantage of the observation that many of thecell growth regulatory mechanisms that control normal cell growth areinactivated or lost in neoplastic cells, and that these same growthcontrol mechanisms are inactivated by viruses to facilitate viralreplication. Thus, the deletion or inactivation of a viral gene thatinactivates a particular normal cell growth control mechanism willprevent the virus from replicating in normal cells, but such viruseswill replicate in and kill neoplastic cells that lack the particulargrowth control mechanism.

[0007] For example, normal dividing cells transiently lack the growthcontrol mechanism, retinoblastoma tumor suppressor, that is lacking inand associated with unrestricted growth in certain neoplastic cells. Theloss of retinoblastoma tumor suppressor gene (RB) gene function has beenassociated with the etiology of various types of tumors. The product ofthis tumor suppressor gene, a 105 kilodalton polypeptide called pRB orp105, is a cell-cycle regulatory protein. The pRB polypeptide inhibitscell proliferation by arresting cells at the G₁ phase of the cell cycle.The pRB protein is a major target of several DNA virus oncoproteins,including adenovirus E1a, SV40 large T Ag, and papillomavirus E7. Theseviral proteins bind and inactivate pRB, and the function of inactivatingpRB is important in facilitating viral replication. The pRB proteininteracts with the E2F transcription factor, which is involved in theexpression of the adenovirus E2 gene and several cellular genes, andinhibits the activity of this transcription factor (Bagchi et al. (1991)Cell 65: 1063; Bandara et al. (1991) Nature 351: 494; Chellappan et al.(1992) Proc. Natl. Acad. Sci. (U.S.A.) 89: 4549.

[0008] The adenovirus, oncoproteins E1a, disrupts the pRB/E2F complexresulting in activation of E2F. However, neoplastic or normal dividingcells lacking sufficient functional pRB to complex E2F will not requirethe presence of a functional oncoprotein, such as E1a, to possesstranscriptionally active E2F. Therefore, it is believed that replicationdeficient adenovirus species which lack the capacity to complex RB butsubstantially retain other essential replicative functions will exhibita replication phenotype in cells which are deficient in RB function(e.g., normal dividing cells, or cells which are homozygous orheterozygous for substantially deleted RB alleles, cells which compriseRB alleles encoding mutant RB proteins which are essentiallynonfunctional, cells which comprise mutations that result in a lack offunction of an RB protein) but will not substantially exhibit areplicative phenotype in non-replicating, non-neoplastic cells. Suchreplication deficient adenovirus species are referred to as E1a-RB⁽⁻⁾replication deficient adenoviruses.

[0009] A cell population (such as a mixed cell culture or a human cancerpatient) which comprises a subpopulation of neoplastic cells anddividing normal cells both lacking RB function, and a subpopulation ofnon-dividing, non-neoplastic cells which express essentially normal RBfunction can be contacted under infective conditions (i.e., conditionssuitable for adenoviral infection of the cell population, typicallyphysiological conditions) with a composition comprising an infectiousdosage of a E1a-RB⁽⁻⁾ replication deficient adenovirus. This results inan infection of the cell population with the E1a-RB⁽⁻⁾ replicationdeficient adenovirus. The infection produces preferential expression ofa replication phenotype in a significant fraction of the cellscomprising the subpopulation of neoplastic and dividing normal cellslacking RB function (RB⁻ cell) but does not produce a substantialexpression of a replicative phenotype in the subpopulation ofnon-dividing neoplastic cells having essentially normal RB function. Theexpression of a replication phenotype in an infected RB⁽⁻⁾ cell(neoplastic or dividing normal cells) results in the death of the cell,such as by cytopathic effect (CPE), cell lysis, apoptosis, and the like,resulting in a selective ablation of such RB⁽⁻⁾ cells from the cellpopulation. See, U.S. Pat. Nos. 5,801,029 and 5,972,706.

[0010] Typically, E1a-RB⁽⁻⁾ replication deficient adenovirus constructssuitable for selective killing of RB(−) neoplastic cells comprisemutations (e.g., deletions, substitutions, frameshifts) which inactivatethe ability of an E1a polypeptide to bind RB protein effectively. Suchinactivating mutations typically occur in the E1a CR1 domain (aminoacids 30-85 in Ad5: nucleotide positions 697-790) and/or the CR2 domain(amino acids 120-139 in Ad5; nucleotide positions 920-967), which areinvolved in binding the p105 RB protein and the p107 protein.Preferably, the CR3 domain (spanning amino acids 150-186) remains and isexpressed as a truncated p289R polypeptide and is functional intransactivation of adenoviral early genes. FIG. 1 portrays schematicallythe domain structure of the E1a-289R polypeptide.

[0011] In addition to alterations in the E1a region of adenovirus, itwould be desirable to enhance viral specific killing of neoplastic cellsthat lack RB function by constructing viruses that have criticalreplicative functions under the control of transcriptionally active E2F.The adenovirus replication cycle has two phases: an early phase, duringwhich 4 transcription units E1, E2, E3, and E4 are expressed, and a latephase which occurs after the onset of viral DNA synthesis when latetranscripts are expressed primarily from the major late promoter (MLP).The late messages encode most of the virus's structural proteins. Thegene products of E1, E2 and E4 are responsible for transcriptionalactivation, cell transformation, viral DNA replication, as well as otherviral functions, and are necessary for viral growth. See, Halbert, D.N., et al., 1985, J Virol. 56:250-7.

[0012] If the adenoviral regions that are involved in virus replicationcould be brought under the control of E2F via an E2F responsivetranscriptional unit, this would provide an enhanced adenovirus thatselectively kills neoplastic cells that lack RB function, but not normalcells.

[0013] By way of background, the following references are presentedrelating to adenoviral vectors with alterations in regions involved inviral replication, including the E4 region, and E2F responsivepromoters.

[0014] WO 98/091563, inventors Branton et al., presents methods andcompositions for using adenoviral E4 proteins for inducing cell death.

[0015] Gao, G-P., et al., describe the use of adenoviral vectors with E1and E4 deletions for liver-directed gene therapy. See, J. Virology,December 1996, p. 8934-8943.

[0016] WO 98/46779 describes certain adenoviral vectors capable ofexpressing a transgene comprising a modified E4 region but retaining E4or f3.

[0017] Yeh, P., et al describe the expression of a minimal E4 functionalunit in 293 cells which permit efficient dual trans-complementation ofadenoviral E1 and E4 regions. See, Yeh, P., et al J. Virology, January1996, pages 559-565.

[0018] U.S. Pat. No. 5,885,833 describes nucleic acid constructscomprising an activator sequence, a promoter module, and a structuralgene. The promoter module comprises a CHR region and a nucleic acidsequence that binds a protein of the E2F family.

[0019] Wang, Q. et al., in Gene Ther. 2:775-83 (1995) describe a 293packaging cell line for propagation of recombinant adenovirus vectorsthat lack E1 and/or E4 regions. To avoid the transactivation effects ofthe E1A gene product in parental 293 cells as well as the overexpression of the E4 genes, the E4 promoter was replaced by a cellularinducible hormone gene promoter, the mouse alpha inhibin promoter.Krougliak and Graham describe the development of cell lines that expressadenovirus type 5 E1, E4, and pIX genes, and thus are able to complementreplication of adenovirus mutants defective in each of these regions.See, Krougliak, V. and Graham, F., Human Gene Therapy, vol. 6: p.1575-1586, 1995. Fang, B., et al. in J. Virol. 71:4798-803 (1997)describe an attenuated, replication incompetent, adenoviral vector thathas the E4 promoter replaced with a synthetic GALA/VP 16 promoter thatfacilitates packaging of the adenoviral vector in 293 cells that stablyexpress the GAL4/VP16 transactivator. The virus was made replicationincompetent by deletion of the E1 region of the virus.

[0020] U.S. Pat. No. 5,670,488 describes adenoviral vectors having oneor more of the E4 open reading frames deleted, but retaining sufficientE4 sequences to promote virus replication in vitro, and having a DNAsequence of interest operably linked to expression control sequences andinserted into the adenoviral genome.

[0021] U.S. Pat. No. 5,882,877 describes adenoviral vectors having theE1, E2, E3 and E4 regions and late genes of the adenovirus genomedeleted and additionally comprising a nucleic acid of interest operablylinked to expression control sequences.

[0022] WO 98/13508 describes selectively targeting malignant cells usingan E2F responsive promoter operably linked to a transgene of interest.

[0023] Neuman, E., et al., show that the transcription of the E2F-1 geneis rendered cell cycle dependent by E2F DNA-binding sites within itspromoter. See, Mol Cell Biol. 15:4660 (1995). Neuman, E., et al alsoshow the structure and partial genomic sequence of the human E2F1 gene.See, Gene. 173:163-9 (1996).

[0024] Parr, M. J., et al., show that tumor-selective transgeneexpression in vivo is mediated by an E2F-responsive adenoviral vector.See, Nat Med. 3:1145-9 (1996). Adams, P. D., and W. G. Kaelin, Jr. showtranscriptional control by E2F. See, Semin Cancer Biol. 6:99-108 (1995).

[0025] Hallenbeck, P., et al., describe vectors for tissue-specificreplication. One such vector is adenovirus that is stated to selectivelyreplicate in a target tissue to provide a therapeutic benefit from thevector per se, or from heterologous gene products expressed from thevector. In the former instance a tissue-specific transcriptionalregulatory sequence is operably linked to a coding region of a gene thatis essential for replication of the vector. Several coding regions aredescribed including E1a, E1B, E2 and E4. See, WO 96/17053 and WO96/17053.

[0026] Henderson, et al., in U.S. Pat. No. 5,698,443 shows an adenovirusvector having at least one of the genes E1A, E1B or E4 under thetranscriptional control of a prostate cell specific response element.

[0027] It should be apparent that viruses offer another means fortreating cancer. Thus, viruses that selectively replicate in, and killneoplastic cells would be an invaluable weapon in a physician's arsenalin the battle against cancer.

SUMMARY OF THE INVENTION

[0028] The invention described herein provides recombinant adenoviralvectors and methods and compositions for constructing the same,preferably replication competent, adenoviral vectors that substantiallyand selectively kill neoplastic cells with little or no killing of nonneoplastic cells that have at least one, and preferably two, adenoviralpromoter regions that control the expression of immediate early genesaltered such that certain transcriptional nucleotide regulatory startsites are removed, or otherwise inactivated, while retaining those sitesthat are required, or that substantially facilitate viral replication,and substituting for the removal of such nucleotide regulatory startsites, a tumor cell specific transcriptional unit, and optionally, aheterologous gene with anti-neoplastic cell activity is substituted fora deleted viral gene.

[0029] The invention further provides recombinant viral vectors andmethods as described above, wherein the adenoviral promoter regions arepreferably the E1a and/or E4, and the heterologous gene is expressedlate in the viral replication cycle, and which heterologous gene isunder the control of adenoviral endogenous gene expression machinery.

[0030] In another aspect, the invention provides adenoviral vectors thatsubstantially and selectively kill neoplastic cells with little or nokilling of non neoplastic cells that have certain E1a and E4 promotertranscriptional nucleotide start sites removed, or otherwiseinactivated, and substituting therefore a tumor cell specifictranscriptional unit.

[0031] In another aspect, the invention provides adenoviral vectors thatsubstantially and selectively kill neoplastic cells with little or nokilling of non neoplastic cells that have at least certain of the E4promoter transcriptional nucleotide start sites removed, or otherwiseinactivated, while retaining those sites that facilitate viralreplication, including certain of the Sp1, ATF, NF1 and NFIII/Oct-1binding sites, and substituting for the E4 promoter nucleotide startsites a tumor cell specific transcriptional unit.

[0032] An object of the invention is a description of an adenoviralvector as described above having the E1a and/or the E4 promotertranscriptional nucleotide start sites removed and substituted thereforea tumor cell specific transcriptional unit wherein such adenoviralvectors further exhibit mutations (e.g., deletions, substitutions,frameshifts) which inactivate the ability of an E1a polypeptide to bindRB protein effectively.

[0033] A further feature of the invention consists of substituting forthe E1a and/or E4 promoter nucleotide start sequences referred to abovewith a tumor cell specific transcriptional unit, one that is responsiveto the pRb signaling pathway, including pRb/p107, E2F-1/-2/-3, G1cyclin/cdk complexes, and preferably the promoter is E2F responsive.

[0034] The invention also presents methods for preventing or treatingdisease, and preferably disease resulting from hyperproliferative cellgrowth, including neoplastic disease using the adenoviral vectorsdescribed herein, alone or in combination with anti-neoplastic agents.

[0035] Yet another feature of the invention is a method for treatingneoplastic disease using adenoviral vectors described above wherein theheterologous gene substituted for a deleted viral gene(s) is expressedlate in the viral replication cycle to enhance the anti-neoplasticactivity of the adenoviral vector.

[0036] The above aspects of the invention, as well as others notdescribed above, will become apparent upon a full consideration of theinvention.

BRIEF DESCRIPTION OF THE DRAWINGS

[0037]FIG. 1 portrays schematically the domain structure of the E1a-289Rpolypeptide.

[0038]FIG. 2 shows the adenoviral E4 promoter.

[0039]FIG. 3 shows diagrammatically the invention E4 shuttle vector andthe position of the restriction sites, SpeI and XhoI, which facilitatessubstitution of the E4 promoter with a promoter of choice.

[0040]FIG. 4 shows (A) Genomic structure of ONYX-443. ONYX-443 has theCD gene inserted into the E3B region of ONYX-411. ONYX-443 also containsa complete deletion of gp19K. (B) in vitro CD expression in cellsinfected with ONYX-443. Human cancer cell lines and cultured normalhuman hepatocytes were infected at an MOI of 1 pfu/cell. At indicatedtime points, cell extracts were prepared and CD protein levels wereanalyzed by immunoblotting analysis.

[0041]FIG. 5 shows CD expression in LNCaP xenograft tumors and liverfollowing intravenous injection of ONYX-443. (A). Virus wereadministrated intravenously through tail vein injection into nude micebearing LNCaP xenograft tumors. Five consecutive daily injections weregiven to each animal at a dose of 2×10⁸ pfu per day. At indicated timepoints (in days, d), animals were sacrificed, tumors and livers wereremoved and analyzed for CD enzymatic activity using a¹⁴C-cytosine-to-uracil conversion assay. The first day of virusadministration was defined as Day 1. C: ¹⁴C-cytosine, U: ¹⁴C-uracil.Each lane represents an individual animal. Top panels: CD activity inLNCaP xenograft tumors. Bottom panels: CD activity in the correspondingmouse livers. 50 μg of total protein was used in each reaction. (B). CDactivity was quantified using an assay that converts¹⁴C-5-fluorocytosine (5-FC) to 5-fluorouracil (5-FU). The amount of 5-FCand 5-FU was determined using a Phospholmager, and percentage of theinput 5-FC that was converted to 5-FU was plotted.

[0042]FIG. 6 shows CD expression in Hep3B and DU145 tumor xenografts andthe corresponding liver following intravenous injection of ONYX-443.Virus injection and animal sample analysis were performed as describedin FIG. 5A. In the Hep3B study ONYX-443 was dosed at 2×10⁸ pfu per dayfor 5 consecutive days (FIG. 6A). In the DU145 study, ONYX-443 was dosedat 5×10⁸ pfu per day for 5 consecutive days (FIG. 6B). At indicated timepoints (in days, d), animals were sacrificed, tumors and livers wereremoved and analyzed for CD enzymatic activity. Each lane represents anindividual animal.

[0043]FIG. 7 shows genomic changes in ONYX-4XX, which collectivelyrefers to ONYX-411, ONYX-451, ONYX-452, and ONYX-455.

[0044]FIG. 8 shows sequence confirmation of ONYX-4XX R2 termini

[0045]FIG. 9 shows Southern blot analysis of certain ONYX-4XX virusesafter serial passage.

[0046]FIG. 10 shows PCR analysis of new species of ONYX-4XX,specifically R3.

[0047]FIG. 11 shows duplication of adenoviral packaging elements, AIthrough AVII. in wild-type adenovirus, and ONYX-4XX viruses, andspecifically in ONYX-451(YCD)-1, ONYX-455(TNF)-1, and ONYX-455(TNF)-2.

DETAILED DESCRIPTION OF THE INVENTION

[0048] All publications, including patents and patent applications,mentioned in this specification are herein incorporated by reference tothe same extent as if each individual publication was specifically andindividually indicated to be incorporated by reference in its entirety.

[0049] Furthermore, it is important to note that while the inventionadenoviral vectors' oncolytic activity is ascribed to a mechanism ofaction involving molecules. in the pRb pathway that affect theexpression of viral genes under the control of an E2F responsivepromoter, the invention should not be construed as limited by thismechanism. Rather it will be appreciated that the invention adenoviralvectors' oncolytic activity is a function of its structural elementswhich are thought to, but may not exert oncolysis through the pRbpathway. Thus, the invention adenoviral vectors derive their tumorversus normal cell killing selectivity by having at least one E2Fresponsive promoter driving either E1a or E4 gene expression. Thepreferred adenoviral vector is one having 2 E2F responsive promoters,one substituted for the E1a promoter and the other for the E4 promoter,as described below.

[0050] Definitions

[0051] Unless defined otherwise, all technical and scientific terms usedherein have the same meaning as commonly understood by one of ordinaryskill in the art to which this invention belongs. Generally, thenomenclature used herein and the laboratory procedures described beloware those well known and commonly employed in the art.

[0052] Standard techniques are used for recombinant nucleic acidmethods, polynucleotide synthesis, and microbial culture andtransformation (e.g., electroporation, lipofection). Generally,enzymatic reactions and purification steps are performed according tothe manufacturer's specifications. The techniques and procedures aregenerally performed according to conventional methods in the art andvarious general references (see generally, Sambrook et al., MolecularCloning: A Laboratory Manual, 2nd. edition (1989) Cold Spring HarborLaboratory Press, Cold Spring Harbor, N.Y.) which are providedthroughout this document. The nomenclature used herein and thelaboratory procedures in analytical chemistry, organic syntheticchemistry, and pharmaceutical formulation described below are those wellknown and commonly employed in the art. Standard techniques are used forchemical syntheses, chemical analyses, pharmaceutical formulation anddelivery, and treatment of patients.

[0053] The phrase “endogenous gene expression machinery” refers to thoseendogenous viral elements responsible for gene expression including, byway of example, nucleotide sequences that comprise promoters, enhancers,alternative splicing sites, alternative translation initiation sites,polyadenylation signals, etc.

[0054] Those skilled in the art will also recognize publications thatfacilitate genetic engineering of the invention adenovirus to producethe invention E1A and/or E4 shuttle vectors. Such would include the workof Hitt, M., et al Construction and propagation of human adenovirusvectors. In: Cell Biology: a Laboratory Handbook; J. Celis (Ed),Academic Press, N.Y. (1996); Graham, F. L. and Prevec, L. Adenovirusbased expression vectors and recombinant vaccines. In: Vaccines: NewApproaches to Immunological Problems. R. W. Ellis (ed) Butterworth. Pp.363-390; and Graham, F. L. and Prevec, L. Manipulation of adenovirusvectors. In: Methods in Molecular Biology, Vol. 7: Gene Transfer andExpression Techniques. E. J. Murray and J. M. Walker (eds) Humana PressInc., Clifton, N.J. pp 109-128, 1991. The materials and methodsdescribed in these articles were or could be used below.

[0055] In the formulae representing selected specific embodiments of thepresent invention, the amino- and carboxy-terminal groups, althoughoften not specifically shown, will be understood to be in the form theywould assume at physiological pH values, unless otherwise specified. Theamino acid residues described herein are preferably in the “L” isomericform. Stereoisomers (e.g., D-amino acids) of the twenty conventionalamino acids, unnatural amino acids such as a,a-distributed amino acids,N-alkyl amino acids, lactic acid, and other unconventional amino acidsmay also be suitable components for polypeptides of the presentinvention, as long as the desired functional property is retained by thepolypeptide. For the peptides shown, each encoded residue whereappropriate is represented by a three letter designation, correspondingto the trivial name of the conventional amino acid, in keeping withstandard polypeptide nomenclature (described in J. Biol. Chem.,243:3552-59 (1969) and adopted at 37 CFR §1.822(b)(2)).

[0056] As employed throughout the disclosure, the following terms,unless otherwise indicated, shall be understood to have the followingmeanings:

[0057] The term “inactivated” as applied to “adenoviral transcriptionalnucleotide regulatory site” sequences means rendering such sequences nonfunctional by mutation, including by deletion of all or part of thesequences, or insertion of other sequences into the adenoviraltranscriptional nucleotide sequences thereby rendering them nonfunctional.

[0058] The term “adenovirus” as referred to herein indicates over 47adenoviral subtypes isolated from humans, and as many from other mammalsand birds. See, Strauss, “Adenovirus infections in humans,” in TheAdenoviruses, Ginsberg, ed., Plenum Press, New York, N.Y., pp. 451-596(1984). The term preferably applies to two human serotypes, Ad2 and Ad5.

[0059] The term “polynucleotide” as referred to herein means a polymericform of nucleotides of at least 10 bases in length, eitherribonucleotides or deoxynucleotides or a modified form of either type ofnucleotide. The term includes single and double stranded forms of DNA.

[0060] The term “oligonucleotide” referred to herein includes naturallyoccurring, and modified nucleotides linked together by naturallyoccurring, and non-naturally occurring oligonucleotide linkages.Oligonucleotides are a polynucleotide subset with 200 bases or fewer inlength. Preferably oligonucleotides are 10 to 60 bases in length.Oligonucleotides are usually single. stranded, e.g. for probes; althougholigonucleotides may be double stranded, e.g. for use in theconstruction of a gene mutant. Oligonucleotides of the invention can beeither sense or antisense oligonucleotides.

[0061] As used herein, the terms “label” or “labeled” refers toincorporation of a detectable marker, e.g., by incorporation of aradiolabeled amino acid or attachment to a polypeptide of biotinylmoieties that can be detected by marked avidin (e.g., streptavidincontaining a fluorescent marker or enzymatic activity that can bedetected by optical or colorimetric methods). Various methods oflabeling polypeptides and glycoproteins are known in the art and may beused.

[0062] By the phrase “tumor cell specific,” as applied to theselectivity of killing of the invention adenoviruses, is meant tumorcells that are killed by the expression of viral genes operably linkedto an E2F responsive promoter. Considering that E2F is expressed bynormal cell, particularly dividing normal cells, it would be expectedthat the invention adenoviruses will also kill dividing normal cells,albeit, to a lesser degree than tumor cells.

[0063] The term “sequence homology” referred to herein describes theproportion of base matches between two nucleic acid sequences or theproportion amino acid matches between two amino acid sequences. Whensequence homology is expressed as a percentage, e.g., 50%, thepercentage denotes the proportion of matches over the length of sequencethat is compared to some other sequence. Gaps (in either of the twosequences) are permitted to maximize matching; gap lengths of 15 basesor less are usually used, 6 bases or less are preferred with 2 bases orless more preferred.

[0064] The term “corresponds to” is used herein to mean that apolynucleotide sequence is homologous (i.e., is identical, not strictlyevolutionarily related) to all or a portion of a referencepolynucleotide sequence, or that a polypeptide sequence is identical toa reference polypeptide sequence. In contradistinction, the term“complementary to” is used herein to mean that the complementarysequence is homologous to all or a portion of a reference polynucleotidesequence. For illustration, the nucleotide sequence “TATAC” correspondsto a reference sequence “TATAC” and is complementary to a referencesequence “GTATA”.

[0065] The following terms are used to describe the sequencerelationships between two or more polynucleotides: “reference sequence”,“comparison window”, “sequence identity”, “percentage of sequenceidentity”, and “substantial identity”. A “reference sequence” is adefined sequence used as a basis for a sequence comparison; a referencesequence may be a subset of a larger sequence, for example, as a segmentof a full-length cDNA or gene sequence given in a sequence listing maycomprise a complete cDNA or gene sequence. Generally, a referencesequence is at least 20 nucleotides in length, frequently at least 25nucleotides in length, and often at least 50 nucleotides in length.Since two polynucleotides may each (1) comprise a sequence (i.e., aportion of the complete polynucleotide sequence) that is similar betweenthe two polynucleotides, and (2) may further comprise a sequence that isdivergent between the two polynucleotides, sequence comparisons betweentwo (or more) polynucleotides are typically performed by comparingsequences of the two polynucleotides over a “comparison window” toidentify and compare local regions of sequence similarity. A “comparisonwindow,” as may be used herein, refers to a conceptual segment of atleast 20 contiguous nucleotide positions wherein a polynucleotidesequence may be compared to a reference sequence of at least 20contiguous nucleotides and wherein the portion of the polynucleotidesequence in the comparison window may comprise additions or deletions(i.e., gaps) of 20 percent or less as compared to the reference sequence(which does not comprise additions or deletions) for optimal alignmentof the two sequences. Optimal alignment of sequences for aligning acomparison window may be conducted by the local homology algorithm ofSmith and Waterman (1981) Adv. Appl. Math. 2: 482, by the homologyalignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity method of Pearson and Lipman (1988)Proc. Natl. Acad. Sci. (U.S.A.) 85: 2444, by computerizedimplementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA inthe Wisconsin Genetics Software Package Release 7.0, Genetics ComputerGroup, 575 Science Dr., Madison, Wis.), or by inspection, and the bestalignment (i.e., resulting in the highest percentage of homology overthe comparison window) generated by the various methods is selected. Theterm “sequence identity” means that two polynucleotide sequences areidentical (i.e., on a nucleotide-by-nucleotide basis) over the window ofcomparison. The term “percentage of sequence identity” is calculated bycomparing two optimally aligned sequences over the window of comparison,determining the number of positions at which the identical nucleic acidbase (e.g., A, T, C, G, U, or I) occurs in both sequences to yield thenumber of matched positions, dividing the number of matched positions bythe total number of positions in the window of comparison (i.e., thewindow size), and multiplying the result by 100 to yield the percentageof sequence identity. The terms “substantial identity” as used hereindenotes a characteristic of a polynucleotide sequence, wherein thepolynucleotide comprises a sequence that has at least 85 percentsequence identity, preferably at least 90 to 95 percent sequenceidentity, more usually at least 99 percent sequence identity as comparedto a reference sequence over a comparison window of at least 20nucleotide positions, frequently over a window of at least 25-50nucleotides, wherein the percentage of sequence identity is calculatedby comparing the reference sequence to the polynucleotide sequence whichmay include deletions or additions which total 20 percent or less of thereference sequence over the window of comparison. The reference sequencemay be a subset of a larger sequence.

[0066] It is important to note that while a preferred embodiment of theinvention is the incorporation of the human E2F-1 promoter, a promoterthat is “substantially identical” is intended to come within thedefinition of an E2F responsive promoter.

[0067] As used herein, “substantially pure” means an object species isthe predominant species present (i.e., on a molar basis it is moreabundant than any other individual species in the composition), andpreferably a substantially purified fraction is a composition whereinthe object species comprises at least about 50 percent (on a molarbasis) of all macromolecular species present. Generally, a substantiallypure composition will comprise more than about 80 percent of allmacromolecular species present in the composition, more preferably morethan about 85%, 90%, 95%, and 99%. Most preferably, the object speciesis purified to essential homogeneity (contaminant species cannot bedetected in the composition by conventional detection methods) whereinthe composition consists essentially of a single macromolecular species.

[0068] The term “polypeptide fragment” or “peptide fragment” as usedherein refers to a polypeptide that has an amino-terminal and/orcarboxy-terminal deletion, but where the remaining amino acid sequenceis identical to the corresponding positions in the naturally-occurringsequence deduced, for example, from a full-length cDNA sequence.Fragments typically 8-10 amino acids long, preferably at least 10-20amino acids long, and even more preferably 20-70 amino acids long.

[0069] By the phrase “pRB pathway,” or “pRb signaling pathway” is meant,at least in part, molecules that affect pRb activity including pRb/p107,E2F-1/-2/-3, and G1 cyclin/cdk complexes. It will be appreciated thatmolecules not presently known may also come within this definition.These molecules mediate their biological effects, at least in part, atthe level of transcription through an E2F responsive promoter.

[0070] Other chemistry terms herein are used according to conventionalusage in the art, as exemplified by The McGraw-Hill Dictionary ofChemical Terms (ed. Parker, S., 1985), McGraw-Hill, San Francisco,incorporated herein by reference.

[0071] The production of proteins from cloned genes by geneticengineering is well known. See, e.g. U.S. Pat. No. 4,761,371 to Bell etal. at column 6, line 3 to column 9, line 65. The discussion whichfollows is accordingly intended as an overview of this field, and is notintended to reflect the full state of the art.

[0072] DNA which encodes proteins may be inserted into the E1A and/or E4adenoviral constructs of the invention, in view of the instantdisclosure, by chemical synthesis, by screening reverse transcripts ofmRNA from appropriate cells or cell line cultures, by screening genomiclibraries from appropriate cells, or by combinations of theseprocedures, as illustrated below. For example, one embodiment of theinvention is the expression of genes that encode prodrug activityenzymes where such genes are incorporated into regions of the inventionadenoviruses that do not affect their ability to replicate. Screening ofmRNA or genomic DNA may be carried out with oligonucleotide probesgenerated from known gene sequence information. Probes may be labeledwith a detectable group.

[0073] In the alternative, a gene sequence may be recovered by use ofthe polymerase chain reaction (PCR) procedure. See U.S. Pat. No.4,683,195 to Mullis et al. and U.S. Pat. No. 4,683,202 to Mullis.

[0074] A vector is a replicable DNA construct, and is used either toamplify DNA encoding a desired protein and/or to express DNA whichencodes the protein. An expression vector is a replicable DNA constructin which a DNA sequence encoding a protein of interest is operablylinked to suitable control sequences capable of effecting the expressionof the protein in a suitable host. The need for such control sequenceswill vary depending upon the host selected and the transformation methodchosen. Generally, control sequences include a transcriptional promoter,an optional operator sequence to control transcription, a sequenceencoding suitable mRNA ribosomal binding sites, and sequences whichcontrol the termination of transcription and translation. Amplificationvectors do not require expression control domains. All that is needed isthe ability to replicate in a host, usually conferred by an origin ofreplication, and a selection gene to facilitate recognition oftransformants.

[0075] DNA regions are operably linked when they are functionallyrelated to each other. For example: a promoter is operably linked to acoding sequence if it controls the transcription of the sequence; aribosome binding site is operably linked to a coding sequence if it ispositioned so as to permit translation. Generally, operably linked meanscontiguous and, in the case of leader sequences, contiguous and inreading frame. A preferred embodiment promoter of the instant inventionin those instances where endogenous adenoviral E1a and/or E4 regionpromoter transcriptional nucleotide regulatory start sites are removedis the substitution with a tumor cell specific promoter, one that isresponsive, directly or indirectly, to molecules in the pRb signalingpathway, including the proteins pRb/p107, E2F-1/-2/-3, G1 cyclin/cdkcomplexes, and preferably the promoter is E2F responsive, and morepreferably the promoter is the human E2F-1.

[0076] By responsive to molecules in the pRb signaling pathway, is meantthe killing of tumor cells caused by the expression of viral genes underthe control an E2F responsive promoter. Suitable host cells for use inthe invention include prokaryotes, yeast cells, or higher eukaryoticcells. Prokaryotes include gram negative or gram positive organisms, forexample Escherichia coli (E. coli) or Bacilli. Higher eukaryotic cellsinclude established cell lines of mammalian origin as described below.Exemplary host cells are DH5a, E. coli W3110 (ATCC No. 27,325), E coliB, E. coli X1776 (ATCC No. 31,537) and E. coli 294 (ATCC No. 31,446).

[0077] Cultures of cells derived from multicellular organisms are adesirable host for recombinant protein synthesis. In principal, anyhigher eukaryotic cell culture is workable, whether from vertebrate orinvertebrate culture. However, mammalian cells are preferred.Propagation of such cells in cell culture has become a routineprocedure. See Tissue Culture, Academic Press, Kruse and Paterson,editors (1973). Examples of useful host cell lines are VERO and HeLacells, Chinese hamster ovary (CHO) cell lines, and FL5.12, W1138, BHK,COS-7, CV, and MDCK cell lines. Expression vectors for such cellsordinarily include (if necessary) an origin of replication, a promoterlocated upstream from the gene to be expressed, along with a ribosomebinding site, RNA splice site (if intron-containing genomic DNA isused), a polyadenylation site, and a transcriptional terminationsequence.

[0078] As used herein, the term “replication deficient virus” refers toa virus that preferentially inhibits cell proliferation, causes celllysis, or induces apoptosis (collectively considered killing) in apredetermined cell population (e.g., tumor cells responsive to moleculesin the pRb signaling pathway) which supports expression of a virusreplication phenotype, and which is substantially unable to inhibit cellproliferation, cause cell lysis, induce apoptosis, or express areplication phenotype in non-replicating, non-transformed cells.

[0079] The term “RB function” refers to the property of having anessentially normal level of a polypeptide encoded by the RB gene (i.e.,relative to non-neoplastic cells of the same histological type), whereinthe RB polypeptide is capable of binding an E1a protein of wild-typeadenovirus 2 or 5. For example, RB function may be lost by production ofan inactive (i.e., mutant) form of RB or by a substantial decrease ortotal loss of expression of pRB polypeptide(s), or by an alteration inone or more of the molecules in the pRb pathway that effect pRb levels.Alternatively, “RB function” refers to the normal transcriptionalactivity of genes, in terms of time of expression and amounts ofproteins expressed, that are under the control of an E2F responsive, pRbpathway sensitive, promoter.

[0080] RB function may be substantially absent in neoplastic cells thatcomprise RB alleles encoding a wild-type RB protein; for example, agenetic alteration outside of the RB locus, such as a mutation thatresults in aberrant subcellular processing or localization of RB, or amolecule in the pRB pathway, may result in a loss of RB function.

[0081] The term “replication phenotype” refers to one or more of thefollowing phenotypic characteristics of cells infected with a virus suchas a replication deficient adenovirus: (1) substantial expression oflate gene products, such as capsid proteins (e.g., adenoviral pentonbase polypeptide) or a heterologous gene that exhibits a late expressionprofile, or RNA transcripts initiated from viral late gene promoter(s),(2) replication of viral genomes or formation of replicativeintermediates, (3) assembly of viral capsids or packaged virionparticles, (4) appearance of cytopathic effect (CPE) in the infectedcell, (5) completion of a viral lytic cycle, and (6) other phenotypicalterations which are typically contingent upon abrogation of RBfunction in non-neoplastic cells infected with a wild-type replicationcompetent DNA virus encoding functional oncoprotein(s). A replicationphenotype comprises at least one of the listed phenotypiccharacteristics, preferably more than one of the phenotypiccharacteristics.

[0082] The term “antineoplastic replication deficient virus” is usedherein to refer to a recombinant virus which has the functional propertyof inhibiting development or progression of a neoplasm in a human, bypreferential cell killing, whether by lysis or apoptosis of infectedneoplastic cells relative to infected non-replicating, non-neoplasticcells of the same histological cell type.

[0083] As used herein, “neoplastic cells” and “neoplasia” refer to cellswhich exhibit relatively autonomous growth, so that they exhibit anaberrant growth phenotype characterized by a significant loss of controlof cell proliferation. Neoplastic cells comprise cells which may beactively replicating or in a temporary non-replicative resting state (G₁or G₀); similarly, neoplastic cells may comprise cells which have awell-differentiated phenotype, a poorly-differentiated phenotype, or amixture of both type of cells. Thus, not all neoplastic cells arenecessarily replicating cells at a given timepoint. The set defined asneoplastic cells consists of cells in benign neoplasms and cells inmalignant (or frank) neoplasms. Frankly neoplastic cells are frequentlyreferred to as tumor cells or cancer cells, typically termed carcinomaif originating from cells of endodermal or ectodermal histologicalorigin, or sarcoma if originating from cell types derived from mesoderm.

[0084] As used herein, “physiological conditions” refers to an aqueousenvironment having an ionic strength, pH, and temperature substantiallysimilar to conditions in an intact mammalian cell or in a tissue spaceor organ of a living mammal. Typically, physiological conditionscomprise an aqueous solution having about 150 mM NaCl (or optionallyKCl), pH 6.5-8.1, and a temperature of approximately 20-45° C.Generally, physiological conditions are suitable binding conditions forintermolecular association of biological macromolecules. For example,physiological conditions of 150 mM NaCl, pH 7.4, at 37° C. are generallysuitable.

Embodiment of the Invention

[0085] The E1a and E4 regions of adenovirus are essential for anefficient and productive infection of human cells. The E1a gene is thefirst viral gene to be transcribed in a productive infection, and itstranscription is not dependent on the action of any other viral geneproducts. However, the transcription of the remaining early viral genesrequires E1a gene expression. The E1a promoter, in addition toregulating the expression of the E1a gene, also integrates signals forpackaging of the viral genome as well as sites required for theinitiation of viral DNA replication. See, Schmid, S. I., and Hearing, P.in Current Topics in Microbiology and Immunology, vol. 199: pages 67-80(1995).

[0086] The invention as applied to E1a adenoviral vectors involves thereplacement of the basic adenovirus E1a promoter, including the CAATbox, TATA box and start site for transcription initiation, with a basicpromoter that exhibits tumor specificity, and preferably is E2Fresponsive, and more preferably is the human E2F-1 promoter. Thus, thisvirus will be repressed in cells that lack molecules, or such moleculesare non functional, that activate transcription from the E2F responsivepromoter. Normal non dividing, or quiescent cells, fall in this class,as the transcription factor, E2F, is bound to pRb, or retinoblastomaprotein, thus making E2F unavailable to bind to and activate the E2Fresponsive promoter. In contrast, cells that contain free E2F shouldsupport E2F based transcription. An example of such cells are neoplasticcells that lack pRb finction, allowing for a productive viral infectionto occur.

[0087] Retention of the enhancer sequences, packaging signals, and DNAreplication start sites which lie in the E1a promoter will ensure thatthe adenovirus infection proceeds to wild type levels in the neoplasticcells that lack pRb function. In essence, the modified E1a promoterconfers tumor specific transcriptional activation resulting insubstantial tumor specific killing, yet provides for enhanced safety innormal cells.

[0088] In creating the E1a adenoviral vector by substituting theendogenous E1a promoter with the.E2F responsive promoter, the elementsupstream of nucleotide 375 in the adenoviral 5 genome are kept intact.The nucleotide numbering is as described by See, Schmid, S. I., andHearing, P. Current Topics in Microbiology and Immunology, vol. 199:pages 67-80 (1995). This includes all of the seven A repeat motifsidentified for packaging of the viral genome (See FIG. 2 of Schmid andHearing, above.) Sequences from nucleotide 375 to nucleotide 536 aredeleted by a BsaAI to BsrBI restriction start site, while stillretaining 23 base pairs upstream of the translational initiation codonfor the E1A protein. An E2F responsive promoter, preferably human E2F-1is substituted for the deleted endogenous E1a promoter sequences usingknown materials and methods. The E2F-1 promoter may be isolated asdescribed in Example 1.

[0089] The E4 region has been implicated in many of the events thatoccur late in adenoviral infection, and is required for efficient viralDNA replication, late mRNA accumulation and protein synthesis, splicing,and the shutoff of host cell protein synthesis. Adenoviruses that aredeficient for most of the E4 transcription unit are severely replicationdefective and, in general, must be propagated in E4 complementing celllines to achieve high titers. The E4 promoter is positioned near theright end of the viral genome and governs the transcription of multipleopen reading frames (ORF). A number of regulatory elements have beencharacterized in this promoter that are critical for mediating maximaltranscriptional activity. In addition to these sequences, the E4promoter region contains regulatory sequences that are required forviral DNA replication. A depiction of the E4 promoter and the positionof these regulatory sequences can be seen in FIGS. 2 and 3.

[0090] Another embodiment of the invention is the generation of anadenoviral vector that has the E4 basic promoter substituted with onethat has been demonstrated to show tumor specificity, preferably an E2Fresponsive promoter, and more preferably the human E2F-1 promoter. Thereasons for preferring an E2F responsive promoter to drive E4 expressionare the same as were discussed above in the context of an E1a adenoviralvector having the E1a promoter substituted with an E2F responsivepromoter. The tumor suppressor function of pRb correlates with itsability to repress E2F-responsive promoters such as the E2F-1 promoter(Adams, P. D., and W. G. Kaelin, Jr. 1995, Cancer Biol. 6:99-108;Sellers, W. R., and W. G. Kaelin. 1996. published erratum appears inBiochim Biophys Acta 1996 Dec 9;1288(3):E-1, Biochim Biophys Acta.1288:M1-5. Sellers, W. R., J. W. Rodgers, and W. G. Kaelin, Jr. 1995,Proc Natl Acad Sci U S A. 92:11544-8.) The human E2F-1 promoter has beenextensively characterized and shown to be responsive to the pRbsignaling pathway, including pRb/p107, E2F-1/-2/-3, and G1 cyclin/cdkcomplexes, and E1A (Johnson, D. G., K. Ohtani, and J. R. Nevins. 1994,Genes Dev. 8:1514-25; Neuman, E., E. K. Flemington, W. R. Sellers, andW. G. Kaelin, Jr. 1995, Mol Cell Biol. 15:4660; Neuman, E., W. R.Sellers, J. A. McNeil, J. B. Lawrence, and W. G. Kaelin, Jr. 1996, Gene.173:163-9.) Most, if not all, of this regulation has been attributed tothe presence of multiple E2F sites present within the E2F-1 promoter.Hence, a virus carrying this (these) modification(s) would be expectedto be attenuated in normal cells that contain an intact (wild type) pRbpathway, yet exhibit a normal infection/replication profile in cellsthat are deficient for pRb's repressive function. In order to maintainthe normal infection/replication profile of this mutant virus we haveretained the inverted terminal repeat (ITR) at the distal end of the E4promoter as this contains all of the regulatory elements that arerequired for viral DNA replication (Hatfield, L. and P. Hearing. 1993, JVirol. 67:3931-9; Rawlins, D. R., P. J. Rosenfeld, R. J. Wides, M. D.Challberg, and T. J. Kelly, Jr. 1984, Cell. 37:309-19; Rosenfeld, P. J.,E. A. O'Neill, R. J. Wides, and T. J. Kelly. 1987, Mol Cell Biol.7:875-86; Wides, R. J., M. D. Challberg, D. R. Rawlins, and T. J. Kelly.1987, Mol Cell Biol. 7:864-74.). This facilitates attaining wild typelevels of virus in pRb pathway deficient tumor cells infected with thisvirus.

[0091] In the invention adenoviral constructs involving the E4 region,the E4 promoter is preferably positioned near the right end of the viralgenome and it governs the transcription of multiple open reading frames(ORFs) (Freyer, G. A., Y. Katoh, and R. J. Roberts. 1984, Nucleic AcidsRes. 12:3503-19; Tigges, M. A., and H. J. Raskas. 1984. Splice junctionsin adenovirus 2 early region 4 mRNAs: multiple splice sites produce 18to 24 RNAs. J Virol. 50:106-17; Virtanen, A., P. Gilardi, A. Naslund, J.M. LeMoullec, U. Pettersson, and M. Perricaudet. 1984, J Virol.51:822-31.) A number of regulatory elements have been characterized inthis promoter that mediate transcriptional activity (Berk, A. J. 1986,Annu Rev Genet. 20:45-79; Gilardi, P., and M. Perricaudet. 1986, NucleicAcids Res. 14:9035-49; Gilardi, P., and M. Perricaudet. 1984, NucleicAcids Res. 12:7877-88; Hanaka, S., T. Nishigaki, P. A. Sharp, and H.Handa. 1987, Mol Cell Biol. 7:2578-87; Jones, C., and K. A. Lee. 1991,Mol Cell Biol. 11:4297-305; Lee, K. A., and M. R. Green. 1987, Embo J.6:1345-53.) In addition to these sequences, the E4 promoter regioncontains elements that are involved in viral DNA replication (Hatfield,L., and P. Hearing. 1993, J Virol. 67:3931-9; Rawlins, D. R., P. J.Rosenfeld, R. J. Wides, M. D. Challberg, and T. J. Kelly, Jr. 1984,Cell. 37:309-19; Rosenfeld, P. J., E. A. O'Neill, R. J. Wides, and T. J.Kelly. 1987, Mol Cell Biol. 7:875-86; Wides, R. J., M. D. Challberg, D.R. Rawlins, and T. J. Kelly. 1987, Mol Cell Biol. 7:864-74.) A depictionof the E4 promoter and the position of these regulatory sequences can beseen in FIGS. 1 and 2. See, also, Jones, C., and K. A. Lee. Mol CellBiol. 11:4297-305 (1991). With these considerations in mind, an E4promoter shuttle was designed by creating two novel restrictionendonuclease sites: a XhoI site at nucleotide 35,576 and a SpeI site atnucleotide 35,815 (see FIG. 3). Digestion with both XhoI and SpeIremoves nucleotides from 35,581 to 35,817. This effectively eliminatesbases −208 to +29 relative to the E4 transcriptional start site,including all of the sequences that have been shown to have maximalinfluence on E4 transcription. In particular, this encompasses the twoinverted repeats of E4F binding sites that have been demonstrated tohave the most significant effect on promoter activation. However, allthree Sp1 binding sites, two of the five ATF binding sites, and both ofthe NF1 and NFIII/Oct-1 binding sites that are critical for viral DNAreplication are retained. Also, many of the E4 promoter elements thatare removed can be substituted with sites that retain similar functions(e.g., transcriptional start site and the TATA box), yet now confertumor cell specificity through the E2F responsive promoter sites.

[0092] The preferred E2F responsive promoter is the human E2F-1promoter. Key regulatory elements in the E2F-1 promoter that mediate theresponse to the pRb pathway have been mapped both in vitro and in vivo(Johnson, D. G., K. Ohtani, and J. R. Nevins. 1994, Genes Dev.8:1514-25; Neuman, E., E. K. Flemington, W. R. Sellers, and W. G.Kaelin, Jr. 1995, Mol Cell Biol. 15:4660; Parr, M. J., Y. Manome, T.Tanaka, P. Wen, D. W. Kufe, W. G. Kaelin, Jr., and H. A. Fine. 1997, NatMed. 3:1145-9.) Thus, we isolated the human E2F-1 promoter fragment frombase pairs −218 to +51, relative to the transcriptional start site, byPCR with primers that incorporated a SpeI and XhoI site into them. Thiscreates the same sites present within the E4 promoter shuttle and allowsfor direct substitution of the E4 promoter with the E2F-1 promoter. Thedetails of the construction of this vector are described more in theExamples.

[0093] One embodiment of the invention is the description of anadenovirus Ela and/or E4 shuttle vector that allows fast and easysubstitution of the endogenous nucleotide transcriptional regulatorysequences, where such sequences are preferably Ela and/or E4 promotersequences, with nucleotide transcriptional regulatory sequences that areresponse to elements (i.e. molecules) in the pRb signaling pathway,including pRb/p107, E2F transcription factors such as E2F-1/-2/-3, andG1 cyclin/cdk complexes. An E1a or E4 adenoviral vector, as describedabove, would be expected to be attenuated in normal cells that containan intact, that is wild type pRb pathway, yet exhibit a normal infectionprofile in cells that are deficient in Rb pathway function, includingfor pRb's repressive function. Due to the presence of the autoregulatoryE2F sites in the E2F-1 promoter, any E1A or E4 adenoviral vector havingnucleotide transcriptional regulatory sequences that are response toelements in the pRb signaling pathway substituted for the endogenous E1aand/or E4 sequences will preferably have a second mutation in theE1A-CR2 (conserved region 2) domain. This is desirable to minimize ElA'sability to disrupt pRb-mediated repression of the E2F elements.

[0094] As referred to above, the adenoviral oncoprotein E1a, disruptsthe pRB/E2F complex resulting in the release and thus the activation ofE2F. The preferred E1a and/or E4 adenovirus shuttle vector construct isone that is mutant in those regions of Ela that bind to pRb and displaceE2F. Thus, suitable E1a-RB replication deficient adenovirus constructsfor use in the methods and compositions of the invention to generate theinvention E1a and/or E4 shuttle vectors include, but are not limited tothe following examples: (1) adenovirus serotype 5 NT dl 1010, whichencodes an E1a protein lacking the CR1 and CR2 domains (deletion ofamino acids 2 to 150; nucleotides 560-1009) necessary for efficient RBbinding, but substantially retaining the CR3 domain (Whyte et al. (1989)Cell 56: 67), and (2) adenovirus serotype 5 dl 312, which comprises adeleted viral genome lacking the region spanning nucleotides 448-1349which encodes the entire E1a region in wild-type adenovirus (Jones N andShenk T (1979) Proc. Natl. Acad. Sci. (U.S.A.) 76: 3665). Ad5 NT dl 1010is a preferred E1a-RB replication deficient adenovirus and is availablefrom Dr. E. Harlow, Massachusetts General Hospital, Boston, Mass.).

[0095] Additional E1a mutants lacking the capacity to bind RB (E1a⁽⁻⁾)can be generated by those of skill in the art by generating mutations inthe E1a gene region encoding E1a polypeptides, typically in the CR1and/or CR2 domains, expressing the mutant E1a polypeptide, contactingthe mutant E1a polypeptides with p105 or a binding fragment of RB underaqueous binding conditions, and identifying mutant E1a polypeptideswhich do not specifically bind RB as being candidate E1a⁽⁻⁾ mutantssuitable for use in the invention. Alternative assays include contactingthe mutant E1a polypeptides with the 300 kD protein and/or p107 proteinor binding fragment thereof under aqueous binding conditions, andidentifying mutant E1a polypeptides which do not specifically bind the300 kD and/or p107 polypeptides as being candidate E1a⁽⁻⁾ mutantssuitable for use in the invention in the production of the E1a and/or E4shuttle vectors. Alternative binding assays include determining theinability of E1a⁽⁻⁾ mutant protein (or absence of E1a protein) to formcomplexes with the transcription factor E2F and/or to lack the abilityto dissociate the RB protein from RB:E2F complexes under physiologicalconditions (Chellappan et al. 1991, Cell, June 14;65(6):1053-61).

[0096] Alternatively, functional assays for determining mutants lackingE1a function, such as loss of transctivation by E1a of transcription ofvarious reporter polypeptides linked to a E1a-dependent transcriptionalregulatory sequence, and the like, will be used. Such inactivatingmutations typically occur in the E1a CR1 domain (amino acids 30-85 inAd5: nucleotide positions 697-790) and/or the CR2 domain (amino acids120-139 in Ad5; nucleotide positions 920-967), which are involved inbinding the p105 RB protein and the p107 protein. Preferably, the CR3domain (spanning amino acids 150-186) remains and is expressed as atruncated p289R polypeptide and is functional in transactivation ofadenoviral early genes.

[0097] It is important to note that while the E2F responsive promoterhuman E2F-1 is the preferred promoter to replace the E1a and/or E4endogenous promoters that any E2F responsive nucleotide sequence that isactivated, directly or indirectly, by elements in the pRb pathway willadequately substitute for the endogenous promoters.

[0098] It is also important to note that while the construction of theE1a and/or E4 adenoviral vectors involves the removal of certaintranscriptional nucleotide start sites that the exact number of suchsites removed or retained should not be construed as limiting theinvention. What is intended in describing the invention is that in theplace of the endogenous promoters, the E2F responsive promoter functionsto drive the E1a and/or E4 genes to kill tumor cells. This process willvary in degree depending on the number or type of transcriptional startsites that are present in the E2F responsive promoter.

[0099] As mentioned above, another aspect of the instant invention isthe incorporation of heterologous genes into the invention adenoviralvectors. The adenovirus replication cycle has two phases: an earlyphase, during which 4 transcription units E1, E2, E3, and E4 areexpressed, and a late phase which occurs after the onset of viral DNAsynthesis when late transcripts are expressed primarily from the majorlate promoter (MLP). See, Halbert, D. N., et al., 1985, J Virol.56:250-7. A desirable feature of the expression of a heterologous geneis that its expression occur late during the adenoviral replicationcycle. Since the invention adenoviral vectors replicate in neoplasticcells where RB function is substantially absent, such heterologous genesare expressed in such neoplastic cells but not in normal cells. Thus,such adenoviral vectors with a heterologous gene have enhancedanti-neoplastic activity, in part attributed to the adenoviral vectorreplicating in the neoplastic cell, and in part attributed to theexpression of the heterologous gene as a late function of adenoviralreplication. Consequently, late expression of the heterologous gene isdirectly linked to neoplastic cell selectivity of adenoviral infection.

[0100] A surprising aspect of the invention adenoviral vectors is thatheterologous genes inserted into the E3 region of the virus, preferablythe E3B region, exhibit an expression pattern similar to genes expressedduring the late phase of infection, that is, expression is dependentupon, or occurs during, viral DNA replication. Thus, while such virusesthat have a heterologous gene inserted in the E3B region are thepreferred embodiments for the expression of heterologous genes, it willbe appreciated that late expression can also be realized by puttingheterologous gene expression under the control of endogenous adenoviralgene expression machinery that regulates late gene expression, such asthe major late promoter.

[0101] It is important to note that while the invention described hereinis presented in terms of adenovirus and an E2F responsive promoter, thatthe invention is not limited to adenovirus. Indeed, the skilledpractitioner of this art will recognize applications to virtually allviruses that exhibit a life cycle similar to adenovirus such that an E2Fresponsive promoter can be incorporated to control the expression ofcertain genes that confer on such viruses selective tumor cell killing.

[0102] Uses of the Invention

[0103] As mentioned above, the invention adenoviruses can be used totreat diseases which have altered pRb pathway function. Additionally,adenoviral therapy of the present invention may be combined with otherantineoplastic protocols, such as conventional chemotherapy, or withother viruses. See U.S. Pat. No. 5,677,178. Chemotherapy may beadministered by methods well known to the skilled practitioner,including systemically, direct injection into the cancer, or bylocalization at the site of the cancer by associating the desiredchemotherapeutic agent with an appropriate slow release material orintra-arterial perfusing the tumor. The preferred chemotherapeutic agentis cisplatin, and the preferred dose may be chosen by the practitionerbased on the nature of the cancer to be treated, and other factorsroutinely considered in administering cisplatin. Preferably, cisplatinwill be administered intravenously at a dose of 50-120 mg/m² over 3-6hours. More preferably it is administered intravenously at a dose of 80mg/m² over 4 hours. A second chemotherapeutic agent, which is preferablyadministered in combination with cisplatin is 5-fluorouracil. Thepreferred dose of 5-fluorouracil is 800-1200 mg/m² per day for 5consecutive days.

[0104] Adenoviral therapy using the instant invention adenoviruses maybe combined with other antineoplastic protocols, such as gene therapy.See, U.S. Pat. No. 5,648,478. As mentioned above, adenovirus constructsfor use in the instant invention will exhibit specific cancer cellkilling. Such constructs may also have prodrug activator genes,including thymidine kinase, cytosine deaminase, or others, that in thepresence of the appropriate prodrug will enchance the antineoplasticeffect of the invention E1a and/or E4 adenovirus vectors. See, U.S. Pat.No. 5,631,236.

[0105] Also, in the event that the instant invention adenoviral mutantselicit an immune response that dampens their effect in a host animal,they can be administered with an appropriate immunosuppressive drug tomaximize their effect. Alternately, a variety of methods exist wherebythe exterior protein coat of adenovirus can be modified to produce lessimmunogenic virus. See, PCT/US98/0503 where it is shown that a majorimmunogenic component of adenovirus' exterior coat, hexon protein, canbe genetically engineered to be less immunogenic. This is done bycreating a chimeric hexon protein by substituting for normal viral hexonprotein epitopes a sequence of amino acids not normally found in hexonprotein. Such adenoviral constructs are less immunogenic than the wildtype virus.

[0106] Another aspect of the instant invention is the incorporation ofheterologous genes with anti-neoplasia activity into the E1a and/or E4shuttle vectors, preferably in the E1B, E3 regions of the virus, morepreferably the E3B region, or in other regions of the virus where theheterologous gene exhibits a late expression pattern. Examples of suchheterologous genes, or fragments thereof that encode biologically activepeptides, include those that encode immunomodulatory proteins, and, asmentioned above, prodrug activators (i.e. cytosine deaminase, thymidinekinase, U.S. Pat. Nos. 5,358,866, and 5,677,178). Examples of the formerwould include interleukin 2, U.S. Pat. Nos. 4,738,927 or 5,641,665;interleukin 7, U.S. Pat. Nos. 4,965,195 or 5,328, 988; and interleukin12, U.S. Pat. No. 5,457,038; tumor necrosis factor alpha, U.S. Pat. Nos.4,677,063 or 5,773,582; interferon gamma, U.S. Pat. Nos. 4,727,138 or4,762,791; or GM-CSF, U.S. Pat. Nos. 5,393,870 or 5,391,485. Additionalimmunomodulatory proteins further include macrophage inflammatoryproteins, including MIP-3, (See, Well, T. N. and Peitsch, M C. J.Leukoc.Biol vol 61 (5): pages 545-50,1997), and cell suicide, or apoptosisinducing proteins, including BAD and BAX. See, Yang, E., et al. Cell,vol 80, pages 285-291 (1995); and Sandeep, R., et al Cell, vol. 91,pages 231-241 (1997). Monocyte chemotatic protein (MCP-3 alpha) may alsobe used. A preferred embodiment of a heterologous gene is a chimericgene consisting of a gene that encodes a protein that traveres cellmembranes, for example, VP22 or TAT, fused to a gene that encodes aprotein that is preferably toxic to cancer but not normal cells. Toincrease the efficacy of the invention adenoviral E1A mutant constructsthey may be modified to exhibit enhanced tropism for particular tumorcell types. For example, as shown in PCT/US98/04964 a protein on theexterior coat of adenovirus may be modified to display a chemical agent,preferably a polypeptide, that binds to a receptor present on tumorcells to a greater degree than normal cells. Also see, U.S. Pat. No.5,770,442 and U.S. Pat. No. 5, 712, 136. The polypeptide can beantibody, and preferably is single chain antibody.

[0107] Purification of Adenoviral Mutants

[0108] Adenovirus is routinely purified by a number of techniquesincluding cesium chloride banding using an ultracentrifuge. However, forlarge scale production of adenovirus, methods which give larger yieldsthan those readily obtainable by cesium chloride ultracentrifugation aredesirable, and involve one or more chromatographic steps. The preferredmethod utilizes ion exchange chromatography. See, for example,PCT/US97/21504; and Huyghe et al., Human Gene Therapy, vol. 6: 1403-1416(1996).

[0109] Formulation

[0110] Adenovirus, including adenoviral mutants, may be formulated fortherapeutic and diagnostic administration to a patient. For therapeuticor prophylactic uses, a sterile composition containing apharmacologically effective dosage of adenovirus is administered to ahuman patient or veterinary non-human patient for treatment, forexample, of a neoplastic condition. Generally, the composition willcomprise about 10³ to 10¹⁵ or more adenovirus particles in an aqueoussuspension. A pharmaceutically acceptable carrier or excipient is oftenemployed in such sterile compositions. A variety of aqueous solutionscan be used, e.g., water, buffered water, 0.4% saline, 0.3% glycine andthe like. These solutions are sterile and generally free of particulatematter other than the desired adenoviral vector. The compositions maycontain pharmaceutically acceptable auxiliary substances as required toapproximate physiological conditions such as pH adjusting and bufferingagents, toxicity adjusting agents and the like, for example sodiumacetate, sodium chloride, potassium chloride, calcium chloride, sodiumlactate, etc. Excipients which enhance infection of cells by adenovirusmay be included.

[0111] Adenoviruses of the invention, or the DNA contained therein, mayalso be delivered to neoplastic cells by liposome or immunoliposomedelivery; such delivery may be selectively targeted to neoplastic cellson the basis of a cell surface property present on the neoplastic cellpopulation (e.g., the presence of a cell surface protein which binds animmunoglobulin in an immunoliposome). Typically, an aqueous suspensioncontaining the virions are encapsulated in liposomes or immunoliposomes.For example, a suspension of adenovirus virions can be encapsulated inmicelles to form immunoliposomes by conventional methods (U.S. Pat. Nos.5,043,164, 4,957,735, 4,925,661; Connor and Huang (1985) J. Cell Biol.101: 582; Lasic D D (1992) Nature 355: 279; Novel Drug Delivery (eds.Prescott L F and Nimmo W S: Wiley, N.Y., 1989); Reddy et al. (1992) J.Immunol. 148: page 1585). Immunoliposomes comprising an antibody thatbinds specifically to a cancer cell antigen (e.g., CALLA, CEA) presenton the cancer cells of the individual may be used to target virions, orvirion DNA to those cells.

[0112] The compositions containing the present adenoviruses or cocktailsthereof can be administered for prophylactic and/or therapeutictreatments of neoplastic disease. In therapeutic application,compositions are administered to a patient already affected by theparticular neoplastic disease, in an amount sufficient to cure or atleast partially arrest the condition and its complications. An amountadequate to accomplish this is defined as a “therapeutically effectivedose” or “efficacious dose.” Amounts effective for this use will dependupon the severity of the condition, the general state of the patient,and the route of administration.

[0113] In prophylactic applications, compositions containing theinvention adenoviruses, or cocktails thereof, are administered to apatient not presently in a neoplastic disease state to enhance thepatient's resistance to recurrence of a cancer or to prolong remissiontime. Such an amount is defined to be a “prophylactically effectivedose.” In this use, the precise amounts again depend upon the patient'sstate of health and general level of immunity.

[0114] The Examples which follow are illustrative of specificembodiments of the invention, and various uses thereof. They are setforth for explanatory purposes only, and are not to be taken as limitingthe invention.

EXAMPLES Example 1

[0115] E2F-1E4 Adenoviral Vector Construction.

[0116] The recombinant plasmid pAd75-100 was obtained from PatrickHearing and contains the Ad5 dl309 fragment from the EcoRI site at 75.9map units (m.u.) to the right end of the viral genome at 100 m.u. (aBamHI linker is located at 100 m.u.) in pBR322 between the EcoRI andBamHI sites. This EcoRI to BamHI fragment was directly subcloned intoLitmus 28 (New England Biolabs) to generate L28:p75-100.dl309. The wildtype Ad5 E3 sequence that is missing in dl309 (Ad5 nucleotides 30,005 to30,750) was restored by replacing the NotI to NdeI fragment in L28:p75-100.dl309 with a wild type NotI to NdeI fragment (Ad5 nucleotides29,510-31,089) from pAd5-SN (described in U.S. Pat. Ser. No. 09/347,604unpublished in-house vector). This plasmid was designatedL28:p75-100.wt. In order to generate the promoter shuttle, a slightlysmaller vector was generated to be the mutagenesis template. PlasmidpKSII+:p94-100 was constructed by directly subcloning the EcoRV to BamHIfragment (Ad5 nucleotides 33,758 to 33,939) from pAD75-100 into pKSII+.A XhoI site at nucleotide 35,577 and a SpeI site at nucleotide 35,816were created using the Stratagene Quickchange site directed mutagenesismethod. The oligonucleotides used to generate these sites were: XhoI(5′-GCTGGTGCCGTCTCGAGTGGTGTTTTTTTAATAGG-3′ and its complement5′-CCTATTAAAAAAACACCACTCGAGACGGCACCAGC-3′) and SpeI(5′-GGGCGGAGTAACTAGTATGTGTTGGG-3′ and its complement 5′CCCAACACATACTAGTTACTCCGCCC-3′). This vector containing both the SpeI andXhoI restriction sites was designated pKSII+:E4PSV. Due to the presenceof both a SpeI and XhoI site in the pKSII+ backbone, the EcoRV to BamHIfragment from pKSII+:E4PSV was subcloned into pRSET (Invitrogen) via thePvuII and BamHI sites and was designated as pRSET:E4PSV. All vectors andpoint mutations were verified by double stranded sequence analysis on anABI automated sequencer.

[0117] The human E2F-1 promoter was isolated by the polymerase chainreaction (PCR) from templates pGL3:E2F-1(−242) and pGL3:E2F-1ΔE2F(−242).pGL3:E2F-1(−242) contains a wild type human E2F-1 promoter out toposition −242 relative to the transcriptional start site.pGL3:E2F-1ΔE2F(−242) contains the same sequences except that both of theE2F binding-site palindromes contain inactivating point mutations. Theprimers used for PCR were as follows: SpeI-E2F1P(5′-GTGAGCACTAGTCGCCTGGTACCATCCGGACAAAGCC-3′) and XhoI-E2F1P(5′-GTGAGCCTCGAGCTCGATCCCGCTCCGCCCCCGG-3′). One hundred nanograms oftemplate DNA were PCR amplified using Pfu DNA polymerase (Stratagene)under the following conditions: an initial denaturation at 98° C. for 5min., followed by 30 cycles of denaturation at 98° C. for 1 min. andannealing/primer extension at 68° C. for 1 min., followed by a finalprimer extension at 68° for 5 min. The PCR products were Qiagenpurified, digested with SpeI and XhoI, gel purified, and ligated intoSpeI and XhoI digested pRSET:E4PSV. These promoter shuttle vectors weredesignated E2F1-E4PSV and E2F1Δ-E4PSV and carry sequences from −218 to+51 relative to the transcriptional start of the human E2F1 promoter.The final vectors used to generate functional virus were created bysubcloning the BstEII to BamHI fragments from both E2F1-E4PSV andE2F1Δ-E4PSV into both L28:p75-100.dl309 and L28:p75-100.wt digested withsame enzymes. These vectors were designated as: E2F1-E4PSV.309,E2F1-E4PSV.wt, E2F1Δ-E4PSV.309, and E2F1Δ-E4PSV.wt. All vectors wereconfirmed by double stranded sequence analysis as described above.

Example 2

[0118] E2F1-E4 Adenovirus Construction.

[0119] Ten micro grams of E2F1-E4PSV.309 were digested with EcoRI andBamHI, treated with calf-intestinal phosphatase, and gel purified. Onemicro gram of EcoRI digested dl922/47 TP-DNA was ligated to ˜5 micrograms of the purified fragment containing the wild type E2F-1 promoterdriving the E4 region overnight at 16° C. Ligations were transfectedinto 293 cells using standard a CaPO₄ transfection method. Briefly, theligated DNA was mixed with 24 micro grams of salmon sperm DNA, 50 microliters of 2.5M CalCl₂, and adjusted to a final volume of 500 microliters with H₂O. This solution was added dropwise to 500 micro liters ofHepes-buffered saline solution, pH 7.05. After standing for 25 minutes,the precipitate was added dropwise to two 60 mm dishes of 293 cellswhich had been grown in DMEM supplemented with 10% fetal bovine serum(FBS) to 60-80% confluency. After 16 hours, the monolayer was washed onetime with phosphate-buffered saline (minus calcium and magnesium)followed by a 5 ml agar overlay consisting of 1% Seaplaque agarose inDMEM supplemented with 2% FBS. Dishes were overlaid with 3-4 ml of theabove agar overlay every 3-4 days until plaques were isolated.

Example 3

[0120] E2F1-E4 Viral Propagation and Confirmation.

[0121] Primary plaques were isolated with a pasteur pipette andpropagated in a 6 well dish on 293 cells in 2 ml of DMEM supplementedwith 2% FBS until the cytopathic effect (CPE) was complete. One-tenth(200 ml) of the viral supernatant was set aside for DNA analysis, whilethe remainder was stored at −80° C. in a cryovial. DNA was isolatedusing Qiagen's Blood Kit as per their recommendation. One-tenth of thismaterial was screened by PCR for the presence of the desired mutationsusing the following primers: for dl922/47(5′-GCTAGGATCCGAAGGGATTGACTTACTCACT-3′ and5′-GCTAGAATTCCTCTTCATCCTCGTCGTCACT-3′) and for the E2F-1 promoter in theE4 region (5′-GGTGACGTAGGTTTTAGGGC-3′ and 5′-GCCATAACAGTCAGCCTTACC-3′).PCR was performed using Clontech's Advantage cDNA PCR kit in a PerkinElmer 9600 machine using the following conditions: an initialdenaturation at 98° C. for 5 min., followed by 30 cycles of denaturationat 98° C. for 1 min. and annealing/primer extension at 68° C. for 3min., followed by a final primer extension at 68° for 5 min. Positiveplaques (as determined by PCR) were subsequently verified by sequenceanalysis. The above PCR products were gel purified and sequenced withthe same primers. Positive plaques were then subjected to a second roundof plaque purification and verified as before. Viruses were propagatedin 293 cells and purified by two rounds of cesium chloride gradientultracentrifugation

Example 4

[0122] E2F1-E1a and E2F1-E1a/E2F1-E4 Vector Construction.

[0123] The human E2F-1 promoter was isolated by the polymerase chainreaction (PCR) from templates pGL3:E2F-1(−242) and pGL3:E2F-1ΔE2F(−242).pGL3:E2F-1(−242) contains a wild type human E2F1 promoter out toposition −242 relative to the transcriptional start site.pGL3:E2F-1ΔE2F(−242) contains the same sequences except that both of theE2F binding-site palindromes contain inactivating point mutations. Theprimers used for PCR were as follows: BamHI-E2F1P(5′-GTGAGCGGATCCGCTCGATCCCGCTCCGCCCCCGG-3′) and HindIII-E2F1P(5′-GTGAGCAAGCTTCGCCTGGTACCATCCGGACAAAGCC-3′). One hundred nanograms oftemplate DNA were PCR amplified using Pfu DNA polymerase (Stratagene)under the following conditions: an initial denaturation at 98° C. for 5min., followed by 30 cycles of denaturation at 98° C. for 1 min. andannealing/primer extension at 68° C. for 1 min., followed by a finalprimer extension at 68° for 5 min. The PCR products were purified overQiaquick columns (Qiagen), digested with BamHI and HindIII, gelpurified, and ligated into BamHI and HindIII partially digestedp922/47-SV (see below). These promoter shuttle vectors were designatedE2F1 wt-922/47.PSV and E2F1Δ-922/47.PSV and carry sequences from −218 to+51 relative to the transcriptional start of the human E2F1 promoter.All vectors were confirmed by double stranded sequence analysis on anABI automated sequencer.

[0124] P922/47-SV is an E1A promoter shuttle vector that also containsan E1A-CR2 deletion from nucleotides 922 to 947. Plasmid P922/47-SV wasconstructed by first digesting pSP64 (Promega) with HindIII, bluntingwith Klenow DNA polymerase, and then religating to generate pSP64 DeltaH3. The 1,737 bp EcoRI to XbaI fragment (containing both Ad5 and pBR322DNA) from pXC1 (Microbix) was then ligated into EcoRI and XbaI digestedpSP64 Delta H3 to generate pSP64-RI/Xba. pSP64-RI/Xba was then digestedwith HindIII and BamHI, blunted with Klenow DNA polymerase and religatedto generate P Delta E1 Delta +. This intramolecular deletion removedsequences from 9529 to 9875 of the pXC1 plasmid, effectively removingthe HindIII, BamHI and ClaI sites. A novel HindIII site at nucleotide376 of Ad5 was then created by digesting P Delta E1 Delta with BsAaI andligating in a HindIII linker (NEB) to generate P Delta E1 Delta +H. Anovel BamHI site was then created at nucleotide 539 of Ad5 by PCRmutagenesis. Two initial PCR reactions were performed. P Delta E1 Delta+H was used as a template with a primer 5′EcoXC1 site present in pBR322and 3′ Bam (5′-CGCGGAATTCTTTTGGATTGAAGCCAATATG-3′) and 3′Bam(5′-CAGTCCCGGTGTCGGATCCGCTCGGAGGAG-3′), whereas plasmid pXC1 (Microbix)was used as the template in a PCR reaction with primers Bsr-Bam(5′-CTCCTCCGAGCGGATCCGACACCGGGACTG-3′) and 3′E1A.Xba(5′-GCGGGACCACCGGGTGTATCTCAGGAGGTG-3′). The PCR products were isolatedon an agarose gel and purified using a Qiagen gel extraction kit. Thetwo PCR products were then mixed and PCR was repeated using the externalmost primers 5′EcoXC1 and 3′E1A.Xba. The resulting 1,400 bp PCR productwas then digested with EcoRI and XbaI and ligated into EcoRI and XbaIdigested P Delta E1 Delta +H to generate Delta E1 Delta +H+B. pXC1-SVwas then constructed by digesting P Delta E1 Delta +H+B with EcoRI andXbaI and ligating the 1,393 bp fragment into EcoRI and XbaI digestedpXC1 (Microbix). Finally, p922/47-SV was generated by using pCIA-922/47(provided by Peter White) as a template for PCR with the followingprimers: Bsr-Bam (5′-CTCCTCCGAGCGGATCCGACACCGGGACTG-3′) and 3′E1A.Xba(5′-GCATTCTCTAGACACAGGTG-3′). The resulting PCR product was purifiedover a Qiagen Qiaquick column, digested with BamHI and XbaI andsubsequently ligated into pXC1-SV that had been digested with BamHI andXbaI.

Example 5

[0125] E2F1-E1a and E2F1-E1a/E2F1-E4Viral Construction.

[0126] ONYX-150 (E2F1 wt-922/47) and ONYX-151 (E2F1 Delta-922/47) weregenerated by cotransfecting 10 micro grams of either E2F1 wt-922/47.PSVor E2F1 Delta-922/47.PSV, respectively, with 10 micro grams of pJM17(Microbix) into 293 cells using a standard CaPO₄ transfection method.ONYX-411 (E2F1 wt-922/47+E2F1 wt-E4) was generated by digesting 10 micrograms of plasmid E2F1-E4PSV.309 (ID-086) with EcoRI and BamHI. Thedigested DNA was then treated with calf-intestinal phosphatase and gelpurified. One microgram of EcoRI digested ONYX-150 (E2F1 wt-922/47)TP-DNA was then ligated to 5 micro grams of the purified fragmentcontaining the wild type E2F-1 promoter driving the E4 region overnightat 16° C. CaPO₄ transfections were performed by mixing the DNA's with 50micro liters of 2.5M CaCl₂ in a final volume of 500 micro liters. In thecase of ONYX-411, the transfection mix contained 24 micrograms of salmonsperm DNA in addition to the ligated DNA's. This solution was addeddropwise to 500 micro liters of Hepes-buffered saline solution, pH 7.05.After standing for 25 minutes, the precipitate was added dropwise to two60 mm dishes of 293 cells which had been grown in DMEM supplemented with10% fetal bovine serum (FBS) to 60-80% confluency. After 16 hours, themonolayer was washed one time with phosphate-buffered saline (minuscalcium and magnesium) followed by a 5 ml agar overlay consisting of 1%Seaplaque agarose in DMEM supplemented with 2% FBS. Dishes were overlaidwith 3-4 ml of the above agar overlay every 3-4 days until plaques wereisolated.

Example 6

[0127] E2F1-E1a and E2F1-E1a/E2F1-E4 Viral Propagation andConfilrmation.

[0128] Primary plaques were isolated with a pasteur pipette andpropagated in a 6 well dish on either 293 or A549 cells in 2 ml of DMEMsupplemented with 2% FBS until the cytopathic effect (CPE) was complete.One-tenth (200 micro liters) of the viral supernatant was set aside forDNA analysis, while the remainder was stored at −80° C. in a cryovial.DNA was isolated using Qiagen's Blood Kit as per their recommendation.One-tenth of this material was screened by PCR for the presence of thedesired mutations using the following sets of primer pairs. The presenceof the human E2F1 promoter driving E1A was confirmed using primersAd5-left (5′-GGGCGTAACCGAGTAAGATTTGGCC-3′) and E1Astart.NC(5′-GGCAGATAATATGTCTCATTTTCAGTCCCGG-3′). The presence of the deletionfrom nucleotides 922 to 947 within E1A was verified using primers Af-7(5-GCTAGGATCCGAAGGGATTGACTTACTCACT-3′) and Af-5 (5′-GCTAGAATTCCTCTTCATCCTCGTCGTCACT-3′). The presence of the human E2F1promoter driving the entire E4 region was confirmed using primersE4.3NCb (5′-GCCATAACAGTCAGCCTTACC-3′) and Ad5-3′end(5′-GGTGACGTAGGTTTTAGGGC-3′). The deletion present in the E3 region(dl309) was confirmed using primers E3.C8(5′-CCTTTATCCAGTGCATTGACTGGG-3′) and 3′-E3I(5′-GGAGAAAGTTTGCAGCCAGG-3′).PCR was performed using Clontech's Advantage cDNA PCR kit in a PerkinElmer 9600 machine using the following conditions: an initialdenaturation at 98° C. for 5 min., followed by 30 cycles of denaturationat 98° C. for 1 min. and annealing/primer extension at 68° C. for 3min., followed by a final primer extension at 68° for 5 min. Positiveplaques (as determined by PCR analysis) were subsequently verified bysequence analysis. The above PCR products were gel purified andsequenced with the same primers. Positive plaques were then subjected toa second round of plaque purification in either 293 or A549 cells andverified exactly as before. Viruses were propagated in 293 cells andpurified by two rounds of cesium chloride gradient ultracentrifugation.All large-scale viral preps were confirmed by the above same PCR andsequence analyses. In addition, all large-scale viral preps wereverified by digestion with either HindIII or XhoI and the fragmentsanalyzed by isolation on a 0.9% agarose gel.

Example 7

[0129] Construction of Onyx-443.

[0130]FIG. 4(A) shows the genomic structure of ONYX-443. It wasconstructed as follows. Plasmid pE3SV+V+B, described in U.S. patentapplication, Ser. No. 09/347,604, and on deposit with the American TypeCulture Collection Bethesda, Md., USA: ATCC No., was used to constructONYX-443. This plasmid contains the E3 region of adenovirus. First, the6.7K and gp 19K genes from the E3 region were deleted by digestingpE3SV+V+B with NheI (28532) and natural MunI (29355) endonucleases,filled in using T4 DNA polymerase, and religated to createpE3SV+V+BΔgp19K plasmid. The NheI and MunI sites were previouslyengineered into pE3SV+V+B.

[0131] Next, the E. coli cytosine deaminase gene (CD) (pCD2, ATCC No.40999, Bethesda, Md., USA) was PCR amplified using primers CD-Cla(5′-CCCCCCAAGCTTATCGATATGTCGAATAAC-3′) and CD-Swa(5′-TCCCCCGGGATTTAAATTCGTTCAACGTTT-3′). The PCR product was purified anddigested with ClaI and SwaI endonucleases and ligated withpE3SV+V+BΔgp19K, which was also digested with ClaI and SwaI to create.E3SV+V+BΔgpl9K+CD(C/S). Note that the bacterial start codon of CD, GTG,was replaced with the eukaryotic start codon, ATG, in the primer design.

[0132] To facilitate homologous recombination with viral DNA, additionaladenovirus sequences were added at the 5′ region ofpE3SV+V+BΔgp19K+CD(C/S). The plasmid was digested with SpeI and ligatedwith the 7533bp fragment isolated from pNB following digestion with NheI(19549) and SpeI (27082) endonucleases to generate pNBΔgp19K-CD(C/S).pNB is described in U.S. patent application, Ser. No. 09/347,604.Orientation of inserted DNA was confirmed by restriction digest sinceNheI and SpeI are compatible cohesive ends.

[0133] Lastly, Onyx-443 was produced by homologous recombination usingviral TP-DNA from ONYX-411, which was digested with EcoRI (Hermiston TW, et al. In: Wold WSM (ed.). Adenovirus Methods and Protocols. HumanaPress: Totowa, N.J., 1999, pp 11-24). Next, pNBΔgp 19K-CD(C/S) wasdigested with BamHI, and the digested plasmid and TP-DNA wereco-transfected in A549 cells using Lipofectamine as described by themanufacturer (Life Technologies), and recombinant virus, ONYX-443 wastriple plaque purified and confirmed by PCR-sequencing using methodsdescribed previously (Hawkins L K et al. Gene Therapy 2001; 8:1123-1131). Viral DNA from CsCl purified ONYX-443 viruses was confirmedby PCR analysis and DNA sequencing of the entire E1 and E3 region inaddition of the E4 region for ONYX-443.

Example 8

[0134] Expression of Cytosine Deaminase in Onyx-443.

[0135] The expression of CD in Onyx 443 was shown to occur both in vitroand in vivo.

[0136] In vitro CD expression. We first compared CD expression incultured tumor cells (C33A, H1299, DU145 and LNCap) and primary normalhuman cells (human hepatocytes, quiescent small airway epithelial cellsand mammary epithelial cells) following infection with ONYX-443 {(FIG.4(B)}. At an MOI of 1, cancer cells infected with ONYX-443 expressedreadily detectable levels of CD at 24 hours post infection. The amountof CD protein increased with time, reaching a maximum level at 72 hourspost infection.

[0137] In contrast to cancer cells, normal cells infected with ONYX-443did not express detectable levels of CD until 72 hours post infection,and the expression levels were significantly lower than in cancer cells.Similar results were obtained from quiescent as well as proliferativenormal human small airway epithelial cells and mammary epithelial cells.The CD expression pattern following ONYX-443 infection was consistentwith the differential replication of the parental ONYX-411 virus intumor cells and normal cells. The CD expressed in these experiments wasfunctional, capable of converting 5-FC to 5-FU in vitro.

[0138] Briefly, immunoblotting was performed as follows. Cultured cellswere infected with at an MOI of 1. At indicated times post-infection,the cells were lysed in 100 mM Tris-Cl [pH 6.8], 5 mM EDTA, 1% SDS, 5%β-mercaptoethanol. For the animal studies, tumor samples were flashfrozen and powderized in liquid nitrogen, and subsequently dissolved inthe same lysis buffer. Cells debris was removed by centrifugation, andsoluble proteins were fractionated by electrophoresis on (12%) pre-castprotein gels (BioWhitaker). After electrophoresis, the proteins wereelectrophoretically transferred to PVDF membranes. Blots were thenincubated with antibodies diluted in PBS containing 1% dry milk and 0.1%Tween-20, and visualized by ECL (Amersham). Anti-CD antibody was diluted1:50,000 [Hawkins, L. K., et al. Gene Ther, 8: 1123-1131, 2001. Rabbitanti-fiber antibody (American Qualex) was diluted 1:1000.

[0139] In vivo CD expression following intravenous virus administration.Next we injected ONYX-443 intravenously through tail vein into nude micecarrying human tumor xenografts, and examined CD activity in xenografttumors and in normal tissues such as liver, lung and spleen. Briefly,tumors were established in nude mice through subcutaneous injection of2×10⁶ tumor cells. When tumors reached an average size of 100 mm³,viruses were administrated intravenously through tail vein injection.Five consecutive daily injections were given to each animal at a dose of2×10⁸ pfu per day, with the exception of the DU145 study, in whichONYX-443 was dosed at 5×10⁸ pfu per day for 5 consecutive days. Thefirst day of virus administration was defined as Day 1. Animals weresacrificed at indicated time points and their tumor and normal tissuesamples were analyzed for CD activity using a cytosine to uracilconversion assay.

[0140] Briefly, the CD assay was conducted as follows. Tumor and liversamples were flash frozen and powderized in liquid nitrogen. Twenty toforty milligrams of the tissue powder was lysed in 20 mM Tris-Cl, pH8.0,0.15 M NaCl, and 1% Triton X-100, and subsequently frozen and thawed forthree times. For cytosine and 5-FC conversion assays, 200 μg of proteinextract was incubated with [2-¹⁴C] cytosine or [2-¹⁴C] 5-fluorocytosine(1 μCi/mmol; Moravek Biochemicals, Brea, Calf.). The reactions weretypically incubated for 2 hours at 37° C. Reaction products wereseparated on thin layer chromatography plates (VWR) and visualized byautoradiography.

[0141] Data from the LNCap xenograft model are shown in FIG. 5A. Twoobservations were made from this study. First, CD activity within tumorsis high in animals injected with ONYX-443, and prolonged over time.Indeed, in animals injected with ONYX-443, tumor CD activity increasedsteadily throughout the entire study. This result is clearlydemonstrated in FIG. 5B, where 5-FC was used as a substrate and theassay was done within the linear range. Second, CD activity in the liverof animals injected with ONYX-443 is low (FIG. 5A). In the vast majorityof animals that received ONYX-443, no liver CD activity was detected.

[0142] CD expression following intravenous virus inoculation wasevaluated in other xenograft mouse models, including Hep3B, DU145 andC33A. In Hep3B tumors, CD expression from ONYX-443 was also high (FIG.6A). The C33A tumor expression pattern was similar to that of the Hep3Bmodel. In DU145 tumors, ONYX-443 demonstrated a sustained high level ofCD activity for at least 24 days (FIG. 6B). In contrast, no CD activitywas detected in livers from animals injected with ONYX-443. Lung andspleen tissues also had no detectable CD activity following intravenousinjection.

[0143] Taken together, ONYX-443 has a favorable in vivo heterologousexpression profile, displaying superior CD activity level in a varietyof tumors as well as better tumor versus liver specificity.

[0144] Correlation Between CD Activity, CD Protein Level and Viral LateGene Expression.

[0145] In order to determine whether the CD activity we detected is areflection of CD protein expression level, we would analyze the animaltumor samples from one typical experiment for both the CD activity andCD protein level. The data would show a correlation between CD enzymaticactivity (converting cytosine to uracil) and CD protein, indicating theCD activity assay reflects the CD gene expression level.

[0146] We also can determine if CD gene expression is correlated withthe replication of ONYX-443, and if so, if the expression of CD is as alate protein. Two experiments could establish that this is the case.First, fiber is a late viral protein whose expression is strictlydependent upon viral DNA replication, and is often used as a marker foradenovirus replication. Therefore we would examine adenovirus fiberexpression in tumor samples taken from mice bearing C33A tumors andinjected intravenously with ONYX-443 as described in FIG. 5A. Atindicated time points, tumor samples are removed and analyzed for CDenzymatic activity using the cytosine-to-uracil conversion assay, andadenovirus fiber protein levels by immunoblotting analysis. The resultswould show a good correlation between CD activity and fiber expression,showing that CD expression is directly linked to the replication of theviral vectors.

[0147] Second, an experiment can be done to show that CD is expressed asan adenoviral late protein. This is done by determining the effects ofaraC (1-B-D-arabinofuranosylcytosine) on CD expression. An importantcharacteristic of adenoviral late protein expression is that it isdependent on viral DNA synthesis. Thus, an experiment to show bonafidelate protein expression is to determine whether or not expression occursin the presence of araC, an inhibitor of DNA replication.

[0148] Thus, araC can be added to the culture medium at a concentrationof 20 micrograms per milliter containing A549 cells, such cells areavailable from the American Type Culture Collection, that are infectedwith ONYX-443 at an m.o.i. of 10 and cell lysates analyzed by Westernblot. The results would show that CD in E3B is a bonafide late proteinas its expression is dependent on DNA replication.

Example 9

[0149] Recombinant Forms of E2F1-E1a/E2F1-E4 Virus

[0150] Onyx-411 (E2F1 wt-922/47+E2F1 wt-E4) was constructed as describedabove in Examples 4 and 5. The genome of ONYX-411 contains two copies ofthe E2F1 promoter, controlling expression of the viral E1A and E4 genes,respectively. It was thus speculated that insertion of this promoter atthese two sites would give rise to homologous recombinant forms ofONYX-411. We observed that two viable viruses result from homologousrecombination of ONYX-411. We have termed these R1, the product ofintra-molecular recombination, and R2, the product of inter-molecularrecombination. There is also an R3 form of the virus discussed in detailbelow.

[0151] In the experiments described below certain virus constructs builton the ONYX-411 backbone were used, and these are: ONYX-451, whichcontains Yeast C. kefyr cytosine deaminase (CD) gene (U.S. PatentProvisional S/N: 60/436,707) in the E3B region, ONYX-452 which containshuman GM-CSF (U.S. Pat. Nos. 5,393,870 or 5,391,485) in the E3B region,and ONYX-455 contains the human TNFalpha gene (U.S. Pat. Nos. 4,677,063or 5,773,582). These viruses were made using pE2F-GBV as follows. First,pL28.WT.E2F1P.E4.309 (described in Johnson et al. Cancer Cell. 1:325-37.2001) was digested to completion with EcoR I and BamH I. The 9 kb viralsequence was purified and subcloned in the EcoR I-BamH I gap ofpGEM-7zf(+) (Promega) to create pGEM.dl309.(75-100).WT.E2F1P. Second,pE3SV+B+V (Hawkins and Hermiston. Gene Ther. 8:1142-1148. 2001) wasdigested to completion with EcoR I and Nde I, and the 3.8 kb viralsequence was purified and used to replace the corresponding fragment inpGEM.dl309.(75-100).WT.E2F1P to generate pE2F-GBV. This second cloningstep introduced a number of unique restriction sites to facilitatesubsequent insertion of the foreign transgenes. The cDNAs for C. kefyrcytosine deaminase, human GM-CSF and human TNF-α were cloned in the ClaI and Swa I-digested pE2F-GBV to generate pE2F-yCD, pE2F-GM andpE2F-TNF, respectively. pE2F-yCD contains wild-type gp19K. pE2F-GM has acomplete deletion of gp19K by digestion with Nhe I and Mun I, filling inwith Klenow, and religation. pE2F-TNF contains HSV thymidine kinase cDNAin place of gp19K by insertion in the Nhe I-Mun I gap. pE2F-yCD, pE2F-GMand pE2F-TNF were used to generate ONYX-451, ONYX-452 and ONYX-455,respectively. Briefly, these plasmids were digested with EcoR I and BamHI, and the 9 kb fragments containing viral sequences were purified andco-transfected with EcoR I-digested ONYX-411 TP-DNA into A549 cells.Transfected cells were allowed to grow under soft agar overlaycontaining standard nutritions. Plaques typically appeared at 6-10 dayspost transfection. Individual plaques were screened for the correctrecombinant virus. Recombinant viruses were confirmed by PCR analysisand DNA sequencing of the entire E1 and E3 regions.

[0152] ONYX-411 carries the inverted terminal repeat-packagingsignal-E2F1 promoter (ITR-Ψ-P) arrangement at its left terminus andinverted terminal repeat-E2F1 promoter (ITR-P) at its right terminus. InR1, this arrangement is reversed, i.e. ITR-P is at the left terminus andITR-Ψ-P at the right terminus of the genome. R2 has ITR-Ψ-P at bothtermini of the genome. These constructs are shown in FIG. 7. In thisfigure ONYX-411 is referred to as R0.

[0153] Based on PCR and Southern blot analysis, both R1 and R2 wereshown to be present in preparations of ONYX-411 (R0), respectively. R1is present in trace amounts, only detectable by PCR, while R2 is presentat up to 20% of the total virus population.

[0154] Experiments were conducted to determine the stability ofONYX-411, R1 and R2. It was speculated that R2 is the more stable thanR1 since it is identical to Onyx 411.

[0155] This was borne out by plaque purifying several R2 viruses whichcontained different transgenes inserted in the E3B region of ONYX-411.Several plaques of the same virus were isolated. The R2 form of ONYX-451contains Yeast C. kefyr cytosine deaminase gene (U.S. Patent ProvisionalS/N: 60/436,707) in the E3B region, while the R2 form of ONYX-452contains human GM-CSF (U.S. Pat. Nos. 5,393,870 or 5,391,485) in the E3Bregion, and the R2 form of ONYX-455 contains the human TNFalpha gene(U.S. Pat. Nos. 4,677,063 or 5,773,582) in the E3B region. The identityof these R2 forms was confirmed by direct DNA sequencing (FIG. 8). Todifferentiate the pure R2 forms from the mixture, we named the originalmixture (containing R0, R1 and R2) the “A” form and the purified R2 the“B” form. We demonstrated that the B form is biologicallyindistinguishable from the A form in progeny production, cytotoxicity,gene expression pattern, tumor vs. normal cells selectivity, etc. Thesedata suggests that the B form retains the same biological activity andoncolytic potency as the A form.

[0156] Finally, in addition to the above, duplication of the packagingsequence, or “A” repeats (Schmid and Hearing: J. of Virology, p.3375-3384, vol. 71, No. 5 1997), at the left end of viral genomeoccurred. There are thought to be seven such packaging elements, AIthrough AVII. Duplication of these elements was shown by Southern blotanalysis when ONYX-411 and its derivatives, collectively referred to asONYX-4XX in FIG. 9, were repeatedly passaged (8 passages) in vitro inA549 cells. The analysis was done on two plaque purified viruses fromeach of ONYX-411, ONYX-451, ONYX-452, and ONYX-455. Southern blotanalysis was done using standard techniques. Briefly, total DNA wasextracted from the cell culture supernant, digested with either BamH Ior Xho I, resolved on 2% agarose gels, and transferred to nylonmembranes. Hybridization was carried out using radio-labeled E2F1promoter sequence as the probe. The results are shown in FIG. 9.

[0157] The Xho I blots show that for the A form, there are 3 bands forboth 411 isolates, A-1 and A-2, and 451, A-1 and A-2 isolates. The topone represents the E2F1 promoter sequence at the left end of the virusgenome. The two lower bands represent the R0 and R1+R2 right termini,respectively. For the two isolates of the B forms of 451, 452, and 455,B-1 and B-2, there are only two visible bands; the top one representsthe E2F1 promoter sequence at the left end of the virus genome while thebottom one represents the R2 right terminus.

[0158] In comparison, the BamH I blots (FIG. 9) yielded two bands; thetop one representing the E2F1 promoter sequence at the right end of thegenome and the 500 bp fragment represents the E2F1 promoter sequence atthe left end of the genome. Additionally, and importantly there is afragment at approximately 100-200 bp larger than the one at 500 bp. Thisfragment appears only at late passages, becoming visible as early as inpassage 5. It is most apparent in ONYX-411A-2, 451B-1, 455B-1, and455B-2, but can also be detected in passage 8 clones.

[0159] To understand this phenomenon, we carried out PCR on selectedclones using primers P3 and P5: P3: 5′ GCCATAACAGTCAGCCTTACC 3′ P5: 5′GGCAGATAATATGTCTCATTTTCAGTCCCGG 3′

[0160] The DNA templates used were purified from passage 8 viruses. ThePCR products were resolved on a 2% agarose gel and visualized byethidium bromide staining (FIG. 10). There were a number of unexpectedfragments of various sizes from the PCR. The most abundant fragmentswere isolated (as indicated by arrows in FIG. 10) and sequenced.

[0161] DNA sequencing revealed a tandem repeat of viral sequences (FIG.11). Of the three clones that we analyzed, one had a 107 bp insertion(451 B-1), one had a 202 bp insertion (455B-1) and the other had a 115bp insertion (455B-2). A closer inspection indicates that all 3duplicated sequences contain part of, or the entire packaging sequenceof adenovirus type 5. These duplicated sequences were next to theoriginal packaging sequence with no gap in between.

[0162] Duplication of packaging sequence is likely the result ofnon-homologous recombination events because multiple bands were detectedby PCR (FIG. 10), indicating different break points were used, which wasconfirmed by the results of DNA sequencing (FIG. 11). All viruses thatcarry a duplication of packaging sequence are collectively referred toherein as the R3 form (FIG. 1).

[0163] The results presented above support the following: 1) R3 couldderive from the A form as well as from the B form. Since the A formcontains predominantly the R0 form, and the ratio of R2 form in the Aform did not change over passages, R3 can derive from the R0 form. Itcan also derive from the R2 form. 2) Duplication of packaging sequencecould also occur to other adenoviruses (eg., wild-type adenovirus,ONYX-015, U.S. Pat. No. 5,677,178, or viruses with a single E2F1promoter such as ONYX-150 described in Example 5, above) if they arecultured under the same conditions. 3) R3 has a growth advantage overR0, R1 or R2 forms, which is a result of additional packaging sequencesthat permits improved packaging efficiency, allowing more viral genometo be assembled into intact virus particles. This is consistent withwhat we observed, that is, a rapid takeover of the virus population bythe R3 form in the serial passaging experiment (FIG. 9), suggesting thatR3 outgrew other species. Thus, adding additional packaging sequencesnot only improves the overall oncolytic activity of ONYX's selectivereplicating adenoviruses, allowing them to replicate and spread moreefficiently, it also could improve manufacturing of any adenovirusproducts (including replication-competent, replication-incompetent, andgutless adenoviruses).

[0164] The invention now being fully described, it will be apparent toone of ordinary-skill in the art that many changes and modifications canbe made thereto without departing from the spirit or scope of theappended claims.

1 25 1 35 DNA Artificial Sequences Adenovirus 1 gctggtgccg tctcgagtggtgttttttta atagg 35 2 35 DNA Artificial Sequences Adenovirus 2cctattaaaa aaacaccact cgagacggca ccagc 35 3 26 DNA Artificial SequencesAdenovirus 3 gggcggagta actagtatgt gttggg 26 4 26 DNA ArtificialSequences Adenovirus 4 cccaacacat actagttact ccgccc 26 5 37 DNAArtificial Sequences Adenovirus 5 gtgagcacta gtcgcctggt accatccggacaaagcc 37 6 34 DNA Artificial Sequences Adenovirus 6 gtgagcctcgagctcgatcc cgctccgccc ccgg 34 7 31 DNA Artificial Sequences Adenovirus 7gctaggatcc gaagggattg acttactcac t 31 8 31 DNA Artificial SequencesAdenovirus 8 gctagaattc ctcttcatcc tcgtcgtcac t 31 9 20 DNA ArtificialSequences Adenovirus 9 ggtgacgtag gttttagggc 20 10 21 DNA ArtificialSequences Adenovirus 10 gccataacag tcagccttac c 21 11 35 DNA ArtificialSequences Adenovirus 11 gtgagcggat ccgctcgatc ccgctccgcc cccgg 35 12 37DNA Artificial Sequences Adenovirus 12 gtgagcaagc ttcgcctggt accatccggacaaagcc 37 13 31 DNA Artificial Sequences Adenovirus 13 cgcggaattcttttggattg aagccaatat g 31 14 30 DNA Artificial Sequences Adenovirus 14cagtcccggt gtcggatccg ctcggaggag 30 15 30 DNA Artificial SequencesAdenovirus 15 ctcctccgag cggatccgac accgggactg 30 16 30 DNA ArtificialSequences Adenovirus 16 gcgggaccac cgggtgtatc tcaggaggtg 30 17 20 DNAArtificial Sequences Adenovirus 17 gcattctcta gacacaggtg 20 18 25 DNAArtificial Sequences Adenovirus 18 gggcgtaacc gagtaagatt tggcc 25 19 31DNA Artificial Sequences Adenovirus 19 ggcagataat atgtctcatt ttcagtcccgg 31 20 31 DNA Artificial Sequences Adenovirus 20 gctaggatcc gaagggattgacttactcac t 31 21 31 DNA Artificial Sequences Adenovirus 21 gctagaattcctcttcatcc tcgtcgtcac t 31 22 21 DNA Artificial Sequences Adenovirus 22gccataacag tcagccttac c 21 23 20 DNA Artificial Sequences Adenovirus 23ggtgacgtag gttttagggc 20 24 24 DNA Artificial Sequences Adenovirus 24cctttatcca gtgcattgac tggg 24 25 20 DNA Artificial Sequences Adenovirus25 ggagaaagtt tgcagccagg 20

We claim
 1. A viral vector comprising an E2F responsive transcriptionalnucleotide regulatory site that controls the expression of a viral gene.2. A viral vector as described in claim 1 wherein said viral gene is animmediate early gene.
 3. A viral vector as described in claim 2 whereinsaid viral vector is adenovirus.
 4. A viral vector as described in claim3, wherein said transcriptional nucleotide regulatory site is apromoter.
 5. A viral vector as described in claim 4, wherein said E2Fresponsive promoter is substituted for an endogenous adenoviral E1apromoter.
 6. A viral vector as described in claim 4, wherein said E2Fresponsive promoter is substituted for an endogenous adenoviral E4promoter.
 7. A viral vector as described in claim 6, wherein said viralvector further comprises nucleotide regulatory sites that substantiallyfacilitate viral replication comprising Sp1, ATF, NF1 and NFIII/Oct-1.8. A viral vector comprising a viral transcriptional nucleotideregulatory site that controls the expression of a viral gene, whereinsaid site is inactivated by the insertion of an E2F responsivetranscriptional nucleotide regulatory site such that said E2F responsivetranscriptional nucleotide regulatory site controls the expression ofsaid viral gene.
 9. A viral vector as described in claim 8 wherein saidviral gene is an immediate early gene.
 10. A viral vector as describedin claim 9 wherein said viral vector is adenovirus.
 11. A viral vectoras described in claim 10, wherein said inactivated transcriptionalnucleotide regulatory site is a promoter.
 12. A viral vector asdescribed in claim 11, wherein said inactivated transcriptionalnucleotide regulatory site is an endogenous adenoviral E1a promoter. 13.A viral vector as described in claim 11, wherein said inactivatedtranscriptional nucleotide regulatory site is an endogenous adenoviralE4 promoter.
 14. A viral vector as described in claim 11, wherein saidinactivated transcriptional nucleotide regulatory site comprises both anendogenous adenoviral E1a and E4 promoters.
 15. An viral vector asdescribed in claims 1 or 8, wherein said transcriptional nucleotideregulatory sequence that is E2F responsive is human E2F-1.
 16. A methodfor killing cancer cells in a population of cancer and normal cells withsubstantially no killing of said normal cells, comprising the steps of:contacting under infective conditions (1) a viral vector as described inclaims 1 or 8 with (2) a cell population comprising said cancer andnormal cells, and allowing sufficient time for said virus to infect saidcell population.
 17. A viral vector as described in claim 1, whereinsaid viral vector is an adenoviral vector, and further comprising aheterologous gene.
 18. A viral vector as described in claim 17, whereinsaid heterologous gene is inserted in a region of the adenoviral genomethat is expressed late during the replication phase of said viralvector.
 19. A viral vector as described in claim 18, wherein saidheterologous gene is inserted in the E3b region of the virus.
 20. Aviral vector as described in claim 19, wherein said heterologous geneexpression is under the control of adenoviral endogenous gene expressionmachinery.
 21. A method for treating cancer in a patient in need of saidtreatment, comprising administering to said patient a viral vector asdescribed in claim
 20. 22. A method as described in claim 21 whereinsaid heterologous gene encodes a protein with anti-cancer activity. 23.A method as described in claim 22 wherein said heterologous gene encodesa protein selected from the group having biological activity consistingof immunomodulatory, pro-drug activator, apoptosis inducing, orchemotatic.
 24. A method for sustained expression of a heterologous genefrom an adenoviral vector, comprising contacting cancer cells with saidadenoviral vector, wherein said adenoviral vector expresses saidheterologous gene late during the adenoviral replication cycle.
 25. Amethod as described in claim 24 wherein said late heterologous geneexpression is under the control of adenoviral endogenous gene expressionmachinery.
 26. A method as described in claim 25 wherein said lateheterologous gene expression is under the control of endogenous geneexpression machinery of the E3 region of adenovirus.
 27. A nucleotidesequence that regulates the expression of an adenoviral early gene(s),comprising an E2F responsive transcriptional nucleotide regulatory siteinserted into or in place of an endogenous adenoviral promoter thatnormally controls the expression of said early gene(s) such that theendogenous adenoviral promoter no longer regulates the expression ofsaid adenoviral early gene(s).
 28. A viral vector as described in claim1 and further comprising more than one viral packaging sequence.
 29. Aviral vector as described in claim 28, wherein said viral vector is anadenoviral vector.
 30. A viral vector as described in claim 29, whereinsaid adenoviral vector is of the R1 form.
 31. A viral vector asdescribed in claim 29, wherein said adenoviral vector is of the R2 form.32. A viral vector as described in claim 29, wherein said adenoviralvector is of the R3 form.
 33. A method for killing tumor cells,comprising contacting said tumor cells with a viral vector of claim 28.34. A viral vector comprising more than one packaging sequence.
 35. Aviral vector as described in claim 34, wherein said viral vector is anadenoviral vector.
 36. A method for killing tumor cells, comprisingcontacting said tumor cells with an adenoviral vector of claim 35.